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

Antisera, Neutralization, Parainfluenza Virus 1-4

21 CFR 866.3400 / Microbiology
FDA source (opens on fda.gov)

GQP is the FDA product code for Antisera, Neutralization, Parainfluenza Virus 1-4, a class I device type, regulated under 21 CFR 866.3400. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GQP
Device name
Antisera, Neutralization, Parainfluenza Virus 1-4
Regulation
21 CFR 866.3400
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
2
Ingested recalls
0

Clearances, product code GQP

By decision year
2 clearances under product code GQP with a decision year between 1994 and 1998, 1994 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code GQP by decision year
YearClearances
19941
19981

Applicants with the most clearances

Product code GQP
Applicants holding the most 510(k) clearances under product code GQP
ApplicantClearances
Dako Diagnostics, Ltd.1
Symex Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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