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

IV FILTERSET 0.22 MICROMETER

K Number: K813446 · Decision Jan 5, 1982
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
43
Review Days
27

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Basic Information

Device Name
IV FILTERSET 0.22 MICROMETER
K Number
K813446
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Imed Corp.
Date Received
December 9, 1981
Decision Date
January 5, 1982
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 Imed Corp.

K Number Device Name
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K950153 VENTED/NONVENTED GEMINI ADMINISTRATION SET WITH CHECK VALVE AND TWO SAFSITE(TM) VALVES
K951922 ADMINISTRATION SETS WITH BALL FLOAT
K950419 THE IMED ORION INFUSION PUMP AND ADMINISTRATION SETS
K944320 VENTED/NON-VENTED GEMINI ADMINISTRATION SET
K945070 VERSASAE PLASTIC CANNULA- 11 GAUGE
K931173 PRIMARY ADMIN SET W/UNIV SP-MAN BELOW/ABV PUMP CH
K933144 GEMINI VOLUMETRIC INFUSION PUMP/CONTROLLER
K924718 SHROUDED NEEDLE DEVICES
Search all 43 clearances from Imed Corp. →