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

LABELING CHANGE FOR CUTTER PUREFLO PLUS IV FILTER

K Number: K880605 · Decision May 26, 1988
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
158
Review Days
104

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Basic Information

Device Name
LABELING CHANGE FOR CUTTER PUREFLO PLUS IV FILTER
K Number
K880605
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
February 12, 1988
Decision Date
May 26, 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

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Other Clearances by Miles Laboratories, Inc.

K Number Device Name
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)
K872634 CUTTER PUREFLO PLUS IV FILTER
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. →