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

GAMBRO-ENGSTROM ERICA IV RESPIRATOR

K Number: K872482 · Decision Mar 3, 1988
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
86
Review Days
254

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Basic Information

Device Name
GAMBRO-ENGSTROM ERICA IV RESPIRATOR
K Number
K872482
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Gambro, Inc.
Date Received
June 23, 1987
Decision Date
March 3, 1988
Product Code
CBK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBK Ventilator, Continuous, Facility Use

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K896758 GAMBRO BICARBONATE MONITOR BCM 10-3
K896757 GAMBRO AK-10 DIALYSIS SYSTEM FOR HIGH FLOWS
K902481 GAMBRO ALWALL GFS PLUS 11, 16 & 20 HOLLOW FIBER
K900918 GAMBRO LUNDIA IC-6H PARALLEL PLATE DIALYZER
K892523 GAMBRO ALWALL GFS 11,12,PLUS 12 HOLLOW FIBER DIALY
K890112 ENGSTROM ELIZA + CO2 ANALYZER
K890111 GAMBRO ALWALL GFE 8 & 9 HOLLOW FIBER DIALYZER
Search all 86 clearances from Gambro, Inc. →