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

Antiserum, Fluorescent, Rabies Virus

21 CFR 866.3460 / Microbiology
FDA source (opens on fda.gov)

GOI is the FDA product code for Antiserum, Fluorescent, Rabies Virus, a class II device type, regulated under 21 CFR 866.3460. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GOI
Device name
Antiserum, Fluorescent, Rabies Virus
Regulation
21 CFR 866.3460
Device class
Class II
Review panel
Microbiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code GOI

By decision year
2 clearances under product code GOI with a decision year between 1982 and 1998, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GOI by decision year
YearClearances
19821
19981

Applicants with the most clearances

Product code GOI
Applicants holding the most 510(k) clearances under product code GOI
ApplicantClearances
Centocor, Inc.1
Light Diagnostics1

Companies listing this code with FDA

Companies whose registered establishments list this code