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Unimed 94720ME

by Unimed Medical Supplies, Inc.

Unimed 94720ME is a Class II device made by Unimed Medical Supplies, Inc., cleared under FDA 510(k) K142832 on 6 Feb 2015 and listed in FDA GUDID since 15 Nov 2022 (UDI-DI 06936735454280), 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) K142832

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 Number06936735454280 UDI-DI Date15 Nov 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK142832 Date6 Feb 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K142832 decided 6 Feb 2015 Active
  • FDA GUDID UDI-DI 06936735454280 listed 15 Nov 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K142832
  2. Listed FDA GUDID 06936735454280

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Unimed
Generic name
Pulse oximeter probe, single-use
Model / reference
94720ME
Primary DI / UDI-DI
06936735454280
510(k) Number
FDA product code
DQA
GMDN term
Pulse oximeter probe, single-use
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Pulse oximeter probe, single-use.

Other devices from Unimed Medical Supplies, Inc.

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Properties

  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)