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

CRITIKON I.V. FILTER

K Number: K842075 · Decision Jun 28, 1984
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
51
Review Days
36

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Basic Information

Device Name
CRITIKON I.V. FILTER
K Number
K842075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Critikon Company, LLC
Date Received
May 23, 1984
Decision Date
June 28, 1984
Product Code
FPB
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
FPB Filter, Infusion Line

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Other Clearances by Critikon Company, LLC

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K982342 DINAMAP MPS SELECT PORTABLE MONITOR
K943709 DINAMAP PLUS VITAL SIGNS MONOITOR
K942700 DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340
K933404 CRITIKON CENTRAL STATIN MONITOR
K933050 CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH
K915697 CRITIKON VITAL SIGNS MODULE
K921295 INTRAVENOUS CATHETERS MODIFICATIONS
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