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

ELISA TOXO IGM

K Number: K914852 · Decision Jan 23, 1992
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
82
Review Days
87

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Basic Information

Device Name
ELISA TOXO IGM
K Number
K914852
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sclavo, Inc.
Date Received
October 28, 1991
Decision Date
January 23, 1992
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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Other Clearances by Sclavo, Inc.

K Number Device Name
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K895847 CREATININE 340 (ENZYMATIC)
K880049 CHOLINESTERASE - BUTYRYTHIOCHOLINE SUBSTRATE
K880199 CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE
K873496 ATYPICAL CHOLINESTERASE
K884035 SAITRON 430 RANDOM ACCESS CHEMISTRY ANALYZER
K884649 TOTAL IRON BINDING CAPACITY TEST
Search all 82 clearances from Sclavo, Inc. →