510(k) K113737
K113737 is an FDA 510(k) premarket notification submitted by Surefire Medical, Inc. for the device "SUREFIRE GUIDE SHEATH". The FDA issued a decision of Substantially Equivalent on Feb 23, 2012. The device falls under product code DQO (Catheter, Intravascular, Diagnostic), a Class II device regulated under 21 CFR 870.1200. Surefire Medical, Inc. has 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 23, 2012
- Date Received
- Dec 20, 2011
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Intravascular, Diagnostic
- Device Class
- Class II
- Regulation Number
- 870.1200
- Review Panel
- CV
- Submission Type
- 510(k)