FDA product code POY
Post Breast Biopsy Hemostatic Breast Compression Device
Radiology·Class 2·21 CFR 892.1710
US regulatory classifications
- US Product Code (FDA)
- POYView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 892.1710View CFR Regulation →
- Medical specialty
- Radiology
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Not Eligible
Definition
To achieve and maintain hemostasis of a breast biopsy wound site.
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About this record
Post Breast Biopsy Hemostatic Breast Compression Device is a medical device type in the Radiology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.