Dravon T Clamp
510(k) K831842
Dravon T Clamp is a Class I device made by Dravon Medical Inc, cleared under FDA 510(k) K831842 on 26 Sep 1983, active as of 8 Nov 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK831842 | Date26 Sep 1983 | StatusActive |
Official records
- FDA 510(k) database K831842
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KDC
- FDA applicant
- Dravon Medical, Inc.
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4800
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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