510(k) K900956
K900956 is an FDA 510(k) premarket notification submitted by Solos Endoscopy, Inc. for the device "GS-7100 CHOLANGIOGRAM CLAMP, 5MM". The FDA issued a decision of Substantially Equivalent on Apr 18, 1990. The device falls under product code GDJ (Clamp, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. Solos Endoscopy, Inc. has 20 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 18, 1990
- Date Received
- Feb 27, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Clamp, Surgical, General & Plastic Surgery
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type
- 510(k) Exempt