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

CHROMATOGRAPHY TUBES

K Number: K790581 · Decision May 15, 1979
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
158
Review Days
49

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Basic Information

Device Name
CHROMATOGRAPHY TUBES
K Number
K790581
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Miles Laboratories, Inc.
Date Received
March 27, 1979
Decision Date
May 15, 1979
Product Code
CDP
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
CDP Radioimmunoassay, Total Triiodothyronine

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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. →