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

ERIKA NEGATIVE PRESSURE ARTERILA BLOOD

K Number: K792053 · Decision Dec 6, 1979
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
76
Applicant Total
43
Review Days
52

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ERIKA NEGATIVE PRESSURE ARTERILA BLOOD
K Number
K792053
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Erika, Inc.
Date Received
October 15, 1979
Decision Date
December 6, 1979
Product Code
FJK
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
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

Similar 510(k) Clearances

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

View all

Other Clearances by Erika, Inc.

K Number Device Name
K853134 NATIONAL MED CARE INFUSION PUMP ADM SET #95-0001-8
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
Search all 43 clearances from Erika, Inc. →