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

TOXONOSTIKA IGM MICROELISA SYSTEM

K Number: K862196 · Decision Sep 11, 1986
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
105
Applicant Total
130
Review Days
94

Basic Information

Device Name
TOXONOSTIKA IGM MICROELISA SYSTEM
K Number
K862196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
ORGANON TEKNIKA CORP.
Date Received
June 9, 1986
Decision Date
September 11, 1986
Product Code
LGD
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

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