510(k) K880726
K880726 is an FDA 510(k) premarket notification submitted by Jms Co., Ltd. for the device "JMS APHERESIS NEEDLE". The FDA issued a decision of Substantially Equivalent on March 16, 1988. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. Jms Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 16, 1988
- Date Received
- February 23, 1988
- Clearance Type
- Traditional
- 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