510(k) K960230
K960230 is an FDA 510(k) premarket notification submitted by Lighthouse Medical, Inc. for the device "SNARE". The FDA issued a decision of Substantially Equivalent on July 31, 1996. The device falls under product code FDI (Snare, Flexible), a Class II device regulated under 21 CFR 876.4300. Lighthouse Medical, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 31, 1996
- Date Received
- January 17, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Snare, Flexible
- Device Class
- Class II
- Regulation Number
- 876.4300
- Review Panel
- GU
- Submission Type