KDM
2007-07-06
Sigmoidoscope, Rigid, Non-Electrical
FDA product code KDM · 1 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.1500
- Review panel
- GU
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2007-07-06 – 2007-07-06
No matching devices.
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