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Cmvgen

by Instrumentation Laboratory CO

510(k) K974456

Cmvgen is a Class II device made by Instrumentation Laboratory CO, cleared under FDA 510(k) K974456 on 1 May 1998, active as of 10 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 10 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 10 Oct 2026.

Regulatory status

as of registry sync 10 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK974456 Date1 May 1998ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
LJO
Device class
Class II
Regulation
21 CFR Part 866.3175
Advisory committee
Microbiology
FDA decision
SESE Substantially Equivalent

Similar devices

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