510(k) K110157
K110157 is an FDA 510(k) premarket notification submitted by JMS North America Corporation for the device "SYSLOC MINI V3". The FDA issued a decision of Substantially Equivalent on February 11, 2011. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. JMS North America Corporation has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 11, 2011
- Date Received
- January 19, 2011
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Fistula
- Device Class
- Class II
- Regulation Number
- 876.5540
- Review Panel
- GU
- Submission Type