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

Prothrombin-Proconvertin And Thrombotest

21 CFR 864.7735 / Hematology
FDA source (opens on fda.gov)

JPF is the FDA product code for Prothrombin-Proconvertin And Thrombotest, a class II device type, regulated under 21 CFR 864.7735. As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
JPF
Device name
Prothrombin-Proconvertin And Thrombotest
Regulation
21 CFR 864.7735
Device class
Class II
Review panel
Hematology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
1

Companies listing this code with FDA

Companies whose registered establishments list this code