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V-Cide VC338

by MicroCare, LLC

V-Cide VC338 (VC338-1) is a Class II device made by MicroCare, LLC, cleared under FDA 510(k) K970726 on 18 May 1998 and listed in FDA GUDID since 26 Oct 2022 (UDI-DI H816MVC3380), active as of 23 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 23 Oct 2026

Documents

510(k) K970726

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberH816MVC3380 UDI-DI Date26 Oct 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK970726 Date18 May 1998DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K970726 decided 18 May 1998 Active
  • FDA GUDID UDI-DI H816MVC3380 listed 26 Oct 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K970726
  2. Listed FDA GUDID H816MVC3380

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
V-Cide
Generic name
Formaldehyde device sterilant
Model / Ref / Catalog
VC338, VC338-1
Primary DI / UDI-DI
H816MVC3380
510(k) Number
FDA product code
MED
GMDN term
Formaldehyde device sterilant
Device class
Class II
Regulation number
880.6885
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MED (Sterilant, Medical Devices).

Other devices from MicroCare, LLC

See all devices from MicroCare, LLC →

Properties

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