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

MPS RESERVOIR BAG

K Number: K982048 · Decision Jul 27, 1998
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
4
Review Days
47

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Basic Information

Device Name
MPS RESERVOIR BAG
K Number
K982048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medical Product Specialists
Date Received
June 10, 1998
Decision Date
July 27, 1998
Product Code
KPE
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KPE Container, I.V.

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K Number Device Name
K982587 MPS FIXED FLOW RATE SET
K982047 MPS HUBER NEEDLE EXTENSION SET
K895367 INTRAVENOUS EXTENSION SET