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

LD-L TRIS SYSTEM PACK TEST

K Number: K820378 · Decision Mar 8, 1982
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
110
Applicant Total
340
Review Days
27

Basic Information

Device Name
LD-L TRIS SYSTEM PACK TEST
K Number
K820378
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1440
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
February 9, 1982
Decision Date
March 8, 1982
Product Code
CFJ
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
CFJ Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase

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