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McKesson 184-FV200

by Mckesson Medical-Surgical Inc.

McKesson 184-FV200 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 9 Jul 2018 (UDI-DI 20612479229321), 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 Number20612479229321 UDI-DI Date9 Jul 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  • Withdrawn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
Fluoride gel
Model / reference
184-FV200
Description
5% Sodium Fluoride Varnish BUBBLEGUM WITH XYLITOL 0.4 mL
Primary DI / UDI-DI
20612479229321
FDA product code
LBH
GMDN term
Fluoride gel
Device class
Class II
Regulation number
872.3260
GUDID distribution status
In Commercial Distribution

Related devices

Category: Fluoride gel

Similar devices

Also classified as Fluoride gel.

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

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