CBG — Spreader, Cuff Class I
FDA product code CBG covers "Spreader, Cuff", a Class I medical device regulated under 21 CFR 868.5760. Submissions are reviewed by the Anesthesiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- CBG
- Device Class
- Class I
- Regulation Number
- 868.5760
- Submission Type
- Review Panel
- AN
- Medical Specialty
- Anesthesiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K870600 | kalajian ent | SOFT EAR STETHOSCOPE | March 19, 1987 |