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PMQClass II

Peripheral Blood Processing Device For Wound Management

21 CFR 864.9245 / Hematology
FDA source (opens on fda.gov)

PMQ is the FDA product code for Peripheral Blood Processing Device For Wound Management, a class II device type, regulated under 21 CFR 864.9245. FDA's definition for this code reads: "Preparation of autologous platelet rich plasma gel from a small sample of peripheral blood for wound management". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
PMQ
Device name
Peripheral Blood Processing Device For Wound Management
FDA definition
Preparation of autologous platelet rich plasma gel from a small sample of peripheral blood for wound management.
Regulation
21 CFR 864.9245
Device class
Class II
Review panel
Hematology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code