FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

JMS APHERESIS NEEDLE SET WINGEATER(R) V2

K Number: K112178 · Decision Oct 27, 2011
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
78
Applicant Total
9
Review Days
91

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Basic Information

Device Name
JMS APHERESIS NEEDLE SET WINGEATER(R) V2
K Number
K112178
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
JMS North America Corporation
Date Received
July 28, 2011
Decision Date
October 27, 2011
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 North America Corporation

K Number Device Name
K251877 JMS CAVEO A.V. Fistula Needle Set
K172499 NEOSHIELD
K151017 JMS Harmony A.V. Fistula Needle Set
K142564 JMS SysLoc MINI A.V. Fistula Needle Set (V4), JMS SysLoc MINI Apheresis Needle Set (V4)
K132321 JMS SYRINGE
K121488 JMS SAFE WING CATH (SWC)
K111948 WINGEATER V2
K110157 SYSLOC MINI V3