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

NATIONAL MED CARE INFUSION PUMP ADM SET #95-0001-8

K Number: K853134 · Decision Nov 6, 1985
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
43
Review Days
103

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Basic Information

Device Name
NATIONAL MED CARE INFUSION PUMP ADM SET #95-0001-8
K Number
K853134
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Erika, Inc.
Date Received
July 26, 1985
Decision Date
November 6, 1985
Product Code
FRN
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
FRN Pump, Infusion

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Other Clearances by Erika, Inc.

K Number Device Name
K852310 NATURALYTE BICARBONATE CONCENTRATE-DRY PACK
K852309 ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1
K850865 TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1-
K850866 TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1L
K850655 TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2
K850654 TORAY INDUS. FILTRYZER HOLLOW FIBER ARTIFICIAL KID
K842436 ERIKA NEGATIVE PRESS. ARTERIAL BLOOD
K831175 FILTRYZER HOLLOW FIBER ARTIF. KIDNEY
K831173 TORAY INDUSTRIES FILTRYZER HOLLOW FIBER
K831176 FILTRYZER HOLLOW FIBER ARTIF. KIDNEY
Search all 43 clearances from Erika, Inc. →