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

Antiserum, Murine Typhus Fever

21 CFR 866.3500 / Microbiology
FDA source (opens on fda.gov)

GPM is the FDA product code for Antiserum, Murine Typhus Fever, a class I device type, regulated under 21 CFR 866.3500. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
GPM
Device name
Antiserum, Murine Typhus Fever
Regulation
21 CFR 866.3500
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 GPM

By decision year
1 clearance under product code GPM with a decision year between 1986 and 1986, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GPM by decision year
YearClearances
19861

Applicants with the most clearances

Product code GPM
Applicants holding the most 510(k) clearances under product code GPM
ApplicantClearances
Health Research, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code GPM.