CYSTOSCOPE— 510(k) K941992
Substantially EquivalentSurgical Technologies, Inc.
FDA 510(k) clearance K941992 for CYSTOSCOPE, Substantially Equivalent on 1995-11-30. Applicant: Surgical Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Surgical Technologies, Inc.
- Product code
- Code FBO
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami Lakes, FL, US
Recent devices under product code FBO
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- K082046 — KARL STORZ PEDIATRIC FLEXIBLE CYSTO-URETHRO-FIBERSCOPE, MODEL 11278C1/ACUI AND CIRCON AUR-735 PEDIATRIC CYSTOURETHEROSCO
- K080780 — ANCHORAGE SCOPE, MODEL 000003
More clearances from Surgical Technologies, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.