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

CHURCHILL 0.22 MICRON LIQUID FILTER SETS

K Number: K880025 · Decision Apr 14, 1988
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
97
Applicant Total
35
Review Days
100

Basic Information

Device Name
CHURCHILL 0.22 MICRON LIQUID FILTER SETS
K Number
K880025
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
CHURCHILL CORP.
Date Received
January 5, 1988
Decision Date
April 14, 1988
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

Similar 510(k) Clearances

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Other Clearances by CHURCHILL CORP.

K Number Device Name
K880051 ENTERAL BAG/SET
K880026 CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETS
K880027 CHURCHILL 1.2 MICRON LIQUID FILTER SET
K870395 CHURCHILL PARENTERAL NUTRITION BAG - EVA
K872585 CHURCHILL-CATH
K872124 CHURCHILL ALBUMIN IV ADMINISTRATION SET
K872123 CHURCHILL TPN ADMINISTRATION SET
K872043 CHURCHILL INTER-CARDIAC SUCKER
K871084 NITROGLYCERINE PUMP SET
K871085 EXTENSION TUBE PUMP SET
Search all 35 clearances from CHURCHILL CORP. →