Tban
510(k) K963252
Tban is a Class II device made by Boston Scientific, cleared under FDA 510(k) K963252 on 20 Sep 1996, active as of 22 Oct 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 | NumberK963252 | Date20 Sep 1996 | StatusActive |
Official records
- FDA 510(k) database K963252
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EOQ
- FDA applicant
- Boston Scientific Corp
- Device class
- Class II
- Regulation
- 21 CFR Part 874.4680
- Advisory committee
- Ear, Nose, Throat
- FDA decision
- SESE Substantially Equivalent
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