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McKesson 900-502MCK

by Mckesson Medical-Surgical Inc.

McKesson 900-502MCK is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 21 Aug 2018 (UDI-DI 20612479234066), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20612479234066 UDI-DI Date21 Aug 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
McKesson
Generic name
Haemoglobin analyser IVD, point-of-care
Model / reference
900-502MCK
Primary DI / UDI-DI
20612479234066
FDA product code
GGM
GMDN term
Haemoglobin analyser IVD, point-of-care
Device class
Class II
Regulation number
864.8625
GUDID distribution status
In Commercial Distribution

Related devices

Category: Haemoglobin analyser IVD, point-of-care

Similar devices in this category

Other devices filed under Haemoglobin analyser IVD, point-of-care.

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)