510(k) K002915
K002915 is an FDA 510(k) premarket notification submitted by Applied Medical for the device "FLEXIBLE OCCLUSION SYSTEM". The FDA issued a decision of Substantially Equivalent on January 8, 2001. The device falls under product code DXC (Clamp, Vascular), a Class II device regulated under 21 CFR 870.4450. Applied Medical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 8, 2001
- Date Received
- September 18, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clamp, Vascular
- Device Class
- Class II
- Regulation Number
- 870.4450
- Review Panel
- CV
- Submission Type