POY
2017-07-19
Post Breast Biopsy Hemostatic Breast Compression Device
FDA product code POY · 1 cleared devices
Class 2
Radiology
- Regulation
- 21 CFR 892.1710
- Review panel
- SU
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2017-07-19 – 2017-07-19
To achieve and maintain hemostasis of a breast biopsy wound site.
No matching devices.
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