510(k) K871965

JMS NEEDLES AND JMS SYRINGES by Jms Co., Ltd. — Product Code FMF

K871965 is an FDA 510(k) premarket notification submitted by Jms Co., Ltd. for the device "JMS NEEDLES AND JMS SYRINGES". The FDA issued a decision of Substantially Equivalent on September 4, 1987. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Jms Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 4, 1987
Date Received
May 19, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Piston
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type