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

MYCOPLASMA IGG ELISA TEST SYSTEM

K Number: K970150 · Decision Jun 16, 1997
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
12
Applicant Total
135
Review Days
152

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Basic Information

Device Name
MYCOPLASMA IGG ELISA TEST SYSTEM
K Number
K970150
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3375
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zeus Scientific, Inc.
Date Received
January 15, 1997
Decision Date
June 16, 1997
Product Code
LJZ
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
LJZ Enzyme Linked Immunoabsorbent Assay, Mycoplasma Spp.

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