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

CUTTER PUREFLO PLUS IV FILTER

K Number: K872634 · Decision Aug 4, 1987
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
158
Review Days
29

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Basic Information

Device Name
CUTTER PUREFLO PLUS IV FILTER
K Number
K872634
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Miles Laboratories, Inc.
Date Received
July 6, 1987
Decision Date
August 4, 1987
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 Miles Laboratories, Inc.

K Number Device Name
K880605 LABELING CHANGE FOR CUTTER PUREFLO PLUS IV FILTER
K874909 MICRO-BUMINTEST REAGENT TABLETS
K875079 MODIFIED SERALYZER ALT/SGPT REAG. STRIPS & MODULE
K871835 GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT
K872120 SERALYZER III BLOOD CHEMISTRY ANALYZER
K873304 CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)
K870214 MODIFIED SALTEX REAGENT STRIPS
K870752 SERALYZER LDH/TOTAL BILIRUBIN/TRIGLYCERIDES STRIPS
K865053 SERA-TEK MICROSOMAL ANTIBODY TEST
K864530 SERALYZER GLUCOSE (HK) REAGENT STRIPS,MODULE,CALI.
Search all 158 clearances from Miles Laboratories, Inc. →