510(k) K962506
K962506 is an FDA 510(k) premarket notification submitted by Gynecare Innovation Center for the device "[SPECIALIZED TISSUE ASPIRATING RESECTOSCOPE (STAR)]". The FDA issued a decision of Substantially Equivalent on September 16, 1996. The device falls under product code FJL (Resectoscope), a Class II device regulated under 21 CFR 876.1500. Gynecare Innovation Center has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 16, 1996
- Date Received
- June 27, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Resectoscope
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type