510(k) K911199

JMS AV FISTULA NEEDLES by Jms Co., Ltd. — Product Code FIE

K911199 is an FDA 510(k) premarket notification submitted by Jms Co., Ltd. for the device "JMS AV FISTULA NEEDLES". The FDA issued a decision of Substantially Equivalent on August 28, 1991. 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 28, 1991
Date Received
March 6, 1991
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