510(k) K990470

JMS A. V. FISTULA NEEDLE SET by Jms Co., Ltd. — Product Code FIE

K990470 is an FDA 510(k) premarket notification submitted by Jms Co., Ltd. for the device "JMS A. V. FISTULA NEEDLE SET". The FDA issued a decision of Substantially Equivalent on August 30, 1999. 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
August 30, 1999
Date Received
February 16, 1999
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