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FDA 510(k) record

K243438

MEMO Patch M (MPT-E08R-UNC01)

510(k) premarket notification. Decision: SESE, 5 December 2025. Product code DXH.

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) numberK243438k_number
Device nameMEMO Patch M (MPT-E08R-UNC01)device_name
ApplicantHuinno Co., Ltd.applicant
Decision date2025-12-05decision_date
DecisionSESEdecision
Product codeDXHproduct_code
Device class2device_class
Review panelnullreview_panel
Clearance typenullclearance_type
Statement or summarynullsummary_type
Regulation numbernullregulation_number
Predicate devicesnullpredicate_devices

Source: FDA openFDA, device/510k, K243438, retrieved 2026-09-19 17:36 Eastern. Public domain (CC0).

Product code

The FDA classification record for the code on this record.

DXH

Transmitters And Receivers, Electrocardiograph, Telephone

Device class 2 · Regulation 870.2920 · Review panel CV

ArrHub vocabulary

Electrophysiology

DXH is one of the 56 product codes in ArrHub’s electrophysiology vocabulary, each held with its FDA classification record as its citation. Vocabulary entry verified 20 September 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: 2026-09-23 07:46 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:K243438&limit=1
{
  "id": "89a8fdd3-a728-4677-8fe6-54a2b30df792",
  "k_number": "K243438",
  "device_name": "MEMO Patch M (MPT-E08R-UNC01)",
  "applicant": "Huinno Co., Ltd.",
  "decision_date": "2025-12-05",
  "decision": "SESE",
  "product_code": "DXH",
  "device_class": "2",
  "review_panel": null,
  "clearance_type": null,
  "summary_type": null,
  "regulation_number": null,
  "predicate_devices": null,
  "source_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243438",
  "verified_at": "2026-09-20T01:33:19.178+00:00",
  "created_at": "2025-12-25T21:24:40.718+00:00",
  "updated_at": "2026-09-19T21:36:08.768714+00:00",
  "collected_at": "2026-09-19T21:36:08.768714+00:00",
  "last_checked_at": null
}

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MEMO Patch M (MPT-E08R-UNC01) — FDA 510(k), 5 December 2025; Health Canada licence none — ArrHub