BSINUS DIAPHANOGRAPH
FDA 510(k) clearance K827448 · decided 1982-05-19
Clearance details
- K-number
- K827448
- Device name
- BSINUS DIAPHANOGRAPH
- Applicant
- Sinus Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-04-22
- Decision date
- 1982-05-19
- Days to decision
- 27 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Ft Lauderdale, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.