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

Antigens, All Groups, Salmonella Spp.

21 CFR 866.3550 / Microbiology
FDA source (opens on fda.gov)

GRL is the FDA product code for Antigens, All Groups, Salmonella Spp., a class II device type, regulated under 21 CFR 866.3550. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GRL
Device name
Antigens, All Groups, Salmonella Spp.
Regulation
21 CFR 866.3550
Device class
Class II
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 GRL

By decision year
2 clearances under product code GRL with a decision year between 1982 and 1995, 1982 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GRL by decision year
YearClearances
19821
19951

Applicants with the most clearances

Product code GRL
Applicants holding the most 510(k) clearances under product code GRL
ApplicantClearances
Fisher Scientific Company L.L.C.1
SA Scientific, Ltd1

Companies listing this code with FDA

Companies whose registered establishments list this code