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CardioDiagnostics Lifesense mini

by Datrix LLC

CardioDiagnostics Lifesense mini (RX93030-006) is a Class II device made by Datrix LLC, cleared under FDA 510(k) K112601 on 9 Nov 2011 and listed in FDA GUDID since 5 Mar 2018 (UDI-DI 00851074007354), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K112601

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851074007354 UDI-DI Date5 Mar 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK112601 Date9 Nov 2011DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K112601 decided 9 Nov 2011 Active
  • FDA GUDID UDI-DI 00851074007354 listed 5 Mar 2018 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K112601
  2. Listed FDA GUDID 00851074007354

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
CardioDiagnostics
Generic name
Telemetric electrocardiographic ambulatory recorder
Model / Ref / Catalog
Lifesense mini, RX93030-006
Primary DI / UDI-DI
00851074007354
510(k) Number
FDA product code
MWJ
GMDN term
Telemetric electrocardiographic ambulatory recorder
Device class
Class II
Regulation number
870.2800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MWJ (Electrocardiograph,Ambulatory(Without Analysis)).

Other devices from Datrix LLC

See all devices from Datrix LLC →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)