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Cavicide Surface Disinfectant/Decontaminant Cleaner

by Micro-Aseptic Products, Inc.

510(k) K951123

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK951123 Date25 Apr 1995ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-2267-2012 FDA Class II initiated 6 Feb 2012

    Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance because the affected lot of product containing this fragance has caused an increase in reported health reactions in some individuals such as headache, nausea, and respiratory discomfort.

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  • Withdrawn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
LRJ
Device Class
Class I
Regulation
21 CFR Part 880.6890
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent