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

Antisera, Cf, Equine Encephalitis Virus, Eee, Wee

21 CFR 866.3240 / Microbiology
FDA source (opens on fda.gov)

GQC is the FDA product code for Antisera, Cf, Equine Encephalitis Virus, Eee, Wee, a class I device type, regulated under 21 CFR 866.3240. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GQC
Device name
Antisera, Cf, Equine Encephalitis Virus, Eee, Wee
Regulation
21 CFR 866.3240
Device class
Class I
Review panel
Microbiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code GQC

By decision year
2 clearances under product code GQC with a decision year between 1992 and 1992, 1992 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code GQC by decision year
YearClearances
19922

Applicants with the most clearances

Product code GQC
Applicants holding the most 510(k) clearances under product code GQC
ApplicantClearances
Hillcrest Biologicals2

Companies listing this code with FDA

Companies whose registered establishments list this code