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

Antiserum, Hai, Mumps Virus

21 CFR 866.3380 / Microbiology
FDA source (opens on fda.gov)

GRD is the FDA product code for Antiserum, Hai, Mumps Virus, a class I device type, regulated under 21 CFR 866.3380. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
GRD
Device name
Antiserum, Hai, Mumps Virus
Regulation
21 CFR 866.3380
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
0

Clearances, product code GRD

By decision year
1 clearance under product code GRD with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GRD by decision year
YearClearances
19841

Applicants with the most clearances

Product code GRD
Applicants holding the most 510(k) clearances under product code GRD
ApplicantClearances
Wellcome Diagnostics1

Companies listing this code with FDA

Companies whose registered establishments list this code