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

MODIFICATION TO JMS APHERESIS NEEDLE

K Number: K000843 · Decision Apr 10, 2000
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
77
Applicant Total
24
Review Days
26

Basic Information

Device Name
MODIFICATION TO JMS APHERESIS NEEDLE
K Number
K000843
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
JMS CO., LTD.
Date Received
March 15, 2000
Decision Date
April 10, 2000
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
K991904 MODIFICATION OF JMS NEEDLES AND JMS SYRINGES
K990470 JMS A. V. FISTULA NEEDLE SET
K990510 JMS APHERESIS NEEDLE
K983707 JMS DIALYZER PRIMING SET
K974902 JMS APHERESIS NEEDLE
Search all 24 clearances from JMS CO., LTD. →