FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

JMS APHERESIS NEEDLE

K Number: K974902 · Decision Mar 30, 1998
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
78
Applicant Total
24
Review Days
90

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Basic Information

Device Name
JMS APHERESIS NEEDLE
K Number
K974902
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jms Co., Ltd.
Date Received
December 30, 1997
Decision Date
March 30, 1998
Product Code
FIE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FIE Needle, Fistula

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FIE), ordered by most recent decision date.

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Other Clearances by Jms Co., Ltd.

K Number Device Name
K002352 JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE
K002394 JMS APHERESIS NEEDLE SET ACCORDION TYPE
K010406 JMS A.V. FISTULA NEEDLE SET WING EATER, MODEL 14G-18G
K010410 JMS APHERESIS NEEDLE WING EATER, MODEL 14G-18G
K000845 MODIFICATION TO JMS A.V. FISTULA NEEDLE SET
K000843 MODIFICATION TO JMS APHERESIS NEEDLE
K991904 MODIFICATION OF JMS NEEDLES AND JMS SYRINGES
K990470 JMS A. V. FISTULA NEEDLE SET
K990510 JMS APHERESIS NEEDLE
K983707 JMS DIALYZER PRIMING SET
Search all 24 clearances from Jms Co., Ltd. →