FDA 510(k) Substantially Equivalent 🇺🇸 United States

DIAGNOSTICS HDL CHOLESTEROL PRECIPITANT

K Number: K821852 · Decision Jul 2, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
340
Review Days
9

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Basic Information

Device Name
DIAGNOSTICS HDL CHOLESTEROL PRECIPITANT
K Number
K821852
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Boehringer Mannheim Corp.
Date Received
June 23, 1982
Decision Date
July 2, 1982
Advisory Committee
Unknown
Review Advisory Committee
CH
Third Party
N

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