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

AMHS BLOOD ANALY. TRIGLYCEOIDES REAG. KI

K Number: K771004 · Decision Sep 12, 1977
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
158
Review Days
102

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AMHS BLOOD ANALY. TRIGLYCEOIDES REAG. KI
K Number
K771004
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Miles Laboratories, Inc.
Date Received
June 2, 1977
Decision Date
September 12, 1977
Product Code
CDT
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
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CDT), ordered by most recent decision date.

View all

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. →