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

SERAQUEST TOXOPLASMA IGM

K Number: K971672 · Decision Oct 21, 1997
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
25
Review Days
167

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Basic Information

Device Name
SERAQUEST TOXOPLASMA IGM
K Number
K971672
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quest Intl., Inc.
Date Received
May 7, 1997
Decision Date
October 21, 1997
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 Quest Intl., Inc.

K Number Device Name
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K023593 SERAQUEST ANTI-THYROID PEROXIDASE (TPO)
K023592 SERAQUEST ANTI-THYROGLOBULIN
K003069 ANTI-CARDIOLIPIN, MULTIPLE AUTOANTIBODIES IMMUNOLOGICAL TEST SYSTEM
K991975 SERAQUEST EB NA IGG
K990410 SERAQUEST EB VCA IGG
K990977 SERAQUEST EB VAC IGM
K982485 SERAQUEST CMV IGM
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