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FDA 510(k) record

K261729

EnSite™ X EP System

510(k) premarket notification. Decision: Substantially Equivalent, 17 September 2026. Product code DQK.

Clearance

Each row is one field of the openFDA record. The grey name is the field’s name in openFDA’s documentation.

FieldValueField name
510(k) numberK261729k_number
Device nameEnSite™ X EP Systemdevice_name
ApplicantAbbott Medicalapplicant
Decision date2026-09-17decision_date
DecisionSubstantially Equivalentdecision
Product codeDQKproduct_code
Device classnulldevice_class
Review panelCardiovascularreview_panel
Clearance typeTraditionalclearance_type
Statement or summarySummarysummary_type
Regulation numbernullregulation_number
Predicate devicesnullpredicate_devices

Source: FDA openFDA, device/510k, K261729, retrieved 2026-10-15 16:01 Eastern. Public domain (CC0).

Product code

The FDA classification record for the code on this record.

DQK

Computer, Diagnostic, Programmable

Device class 2 · Regulation 870.1425 · Review panel CV

ArrHub vocabulary

Electrophysiology

DQK is one of the 60 product codes in ArrHub’s electrophysiology vocabulary, each held with its FDA classification record as its citation. Vocabulary entry verified 13 October 2026.

ArrHub

What ArrHub adds to the record. Everything above this line is the agency’s; everything here is ArrHub’s, dated and attributed.

Resolution

No verified alias in ArrHub’s table; the name stands as the register spells it.

First seen by ArrHub’s weekly snapshot: 2026-10-15 17:24 Eastern.

Raw record

The stored record exactly as ArrHub holds it, for anyone who wants to check the page against it.

Show the raw record (JSON)device/510k.json?search=k_number:K261729&limit=1
{
  "id": "78f48e48-7632-4302-b731-e870eac107b2",
  "k_number": "K261729",
  "device_name": "EnSite™ X EP System",
  "applicant": "Abbott Medical",
  "decision_date": "2026-09-17",
  "decision": "Substantially Equivalent",
  "product_code": "DQK",
  "device_class": null,
  "review_panel": "Cardiovascular",
  "clearance_type": "Traditional",
  "summary_type": "Summary",
  "regulation_number": null,
  "predicate_devices": null,
  "source_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261729",
  "verified_at": "2026-10-15T21:15:17.614+00:00",
  "created_at": "2026-10-15T20:01:33.219923+00:00",
  "updated_at": "2026-10-15T20:01:32.234+00:00",
  "collected_at": "2026-10-15T20:01:32.234+00:00",
  "last_checked_at": "2026-10-15T21:15:17.614+00:00"
}

The readable page is rendered from the record held in ArrHub’s verified view; the agency record at api.fda.gov governs where they differ.

Links open the agency’s own records. Unlabelled links open web pages. Links marked (JSON) open an agency’s data record, which a browser shows as plain text.

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© 2026 ArrHub. Content made available under licence.

EnSite™ X EP System — FDA 510(k), 17 September 2026; Health Canada licence none — ArrHub