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

LD-1

K Number: K900107 · Decision Jan 18, 1990
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
340
Review Days
9

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Basic Information

Device Name
LD-1
K Number
K900107
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.5560
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Boehringer Mannheim Corp.
Date Received
January 9, 1990
Decision Date
January 18, 1990
Product Code
DET
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DET Lactic Dehydrogenase, Antigen, Antiserum, Control

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