510(k) K904797
K904797 is an FDA 510(k) premarket notification submitted by Surgitek for the device "SURGITEK GRADUATED CYSTOSCOPE (MODEL GC-16)". The FDA issued a decision of Substantially Equivalent on March 5, 1991. The device falls under product code FBO (Cystourethroscope), a Class II device regulated under 21 CFR 876.1500. Surgitek has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 5, 1991
- Date Received
- October 23, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cystourethroscope
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type