CYSTOSCOPE
FDA 510(k) clearance K941992 · decided 1995-11-30
Clearance details
- K-number
- K941992
- Device name
- CYSTOSCOPE
- Applicant
- Surgical Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1994-04-25
- Decision date
- 1995-11-30
- Days to decision
- 584 days
- Clearance type
- Traditional
- Product code
- FBO
- Device class
- 2
- Regulation number
- 876.1500
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Miami Lakes, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.