FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CLINITEK 10 SEMI-AUTO URINALYSIS SYS

K Number: K842238 · Decision Jul 25, 1984
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
45
Applicant Total
158
Review Days
50

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Basic Information

Device Name
CLINITEK 10 SEMI-AUTO URINALYSIS SYS
K Number
K842238
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2900
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Miles Laboratories, Inc.
Date Received
June 5, 1984
Decision Date
July 25, 1984
Product Code
KQO
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KQO Automated Urinalysis System

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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)
K872634 CUTTER PUREFLO PLUS IV FILTER
K870214 MODIFIED SALTEX REAGENT STRIPS
K870752 SERALYZER LDH/TOTAL BILIRUBIN/TRIGLYCERIDES STRIPS
K865053 SERA-TEK MICROSOMAL ANTIBODY TEST
Search all 158 clearances from Miles Laboratories, Inc. →