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McKesson 24-807

by Mckesson Medical-Surgical Inc.

McKesson 24-807 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 5 Oct 2018 (UDI-DI 00612479105720), 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 Number00612479105720 UDI-DI Date5 Oct 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  • Withdrawn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
Cotton pledget applicator, single-use
Model / reference
24-807
Primary DI / UDI-DI
00612479105720
FDA product code
KCJ
GMDN term
Cotton pledget applicator, single-use
Device class
Class I
Regulation number
874.5220
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cotton pledget applicator, single-use

Similar devices

Also classified as Cotton pledget applicator, single-use.

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)