TBAN
FDA 510(k) clearance K963252 · decided 1996-09-20
Clearance details
- K-number
- K963252
- Device name
- TBAN
- Applicant
- Boston Scientific Corp
- Decision
- Substantially Equivalent
- Date received
- 1996-08-19
- Decision date
- 1996-09-20
- Days to decision
- 32 days
- Clearance type
- Traditional
- Product code
- EOQ
- Device class
- 2
- Regulation number
- 874.4680
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Natick,, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.