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Pulse oximeter MP-OX150-US

by Better Basics, Inc.

Pulse oximeter MP-OX150-US is a Class II device made by Better Basics, Inc., cleared under FDA 510(k) K082641 on 10 Nov 2008 and listed in FDA GUDID since 18 Nov 2016 (UDI-DI 00817746020151), 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) K082641

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 Number00817746020151 UDI-DI Date18 Nov 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK082641 Date10 Nov 2008DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K082641 decided 10 Nov 2008 Active
  • FDA GUDID UDI-DI 00817746020151 listed 18 Nov 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K082641
  2. Listed FDA GUDID 00817746020151

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Pulse oximeter
Generic name
Pulse oximeter
Model / reference
MP-OX150-US
Primary DI / UDI-DI
00817746020151
510(k) Number
FDA product code
DQA
GMDN term
Pulse oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse oximeter

Cleared under the same submission (K082641)

and 8 more cleared under K082641

Similar devices in this category

Other devices filed under Pulse oximeter.

Other devices from Better Basics, Inc.

See all devices from Better Basics, Inc. →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)