510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K875101Substantially Equivalent

Virogen Cmv Antibody Test

Wampole Laboratories, Cranbury NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K875101 is the FDA 510(k) clearance record for VIROGEN CMV ANTIBODY TEST, a class I device, cleared for Wampole Laboratories on under FDA product code LQO (Dna-Reagents, Campylobacter Spp.). FDA records list 12 510(k) clearances for Wampole Laboratories, from to . As of , FDA records show no recalls naming K875101.

Clearance record

Decision date
Received
(82 days to decision)
Product code
LQO Dna-Reagents, Campylobacter Spp.
Regulation
21 CFR 866.3110
Device class
Class I
Review panel
Microbiology
Applicant
Wampole Laboratories P.O. Box # 1, Cranbury NJ
Third party review
No

Clearances, product code LQO

Trailing 12 months

FDA records hold no clearances under product code LQO in the trailing twelve months.

FDA records show no clearances under product code LQO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LQO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260