510(k) K051814
K051814 is an FDA 510(k) premarket notification submitted by Jms North America Corp. for the device "JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET". The FDA issued a decision of Substantially Equivalent on August 4, 2005. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. Jms North America Corp. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 4, 2005
- Date Received
- July 5, 2005
- 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