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

Antisera, Agglutinating, B. Pertussis, All

21 CFR 866.3065 / Microbiology
FDA source (opens on fda.gov)

GOY is the FDA product code for Antisera, Agglutinating, B. Pertussis, All, a class I device type, regulated under 21 CFR 866.3065. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
GOY
Device name
Antisera, Agglutinating, B. Pertussis, All
Regulation
21 CFR 866.3065
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
1
Ingested recalls
1

Clearances, product code GOY

By decision year
1 clearance under product code GOY with a decision year between 1978 and 1978, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GOY by decision year
YearClearances
19781

Applicants with the most clearances

Product code GOY
Applicants holding the most 510(k) clearances under product code GOY
ApplicantClearances
Absorbent Cotton Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code