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

DIAMEDIX IS-MEASLES IGG TEST SYSTEM

K Number: K974552 · Decision Jan 28, 1998
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
68
Review Days
55

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Basic Information

Device Name
DIAMEDIX IS-MEASLES IGG TEST SYSTEM
K Number
K974552
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3520
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diamedix Corp.
Date Received
December 4, 1997
Decision Date
January 28, 1998
Product Code
LJB
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
LJB Enzyme Linked Immunoabsorbent Assay, Rubeola Igg

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Other Clearances by Diamedix Corp.

K Number Device Name
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K013956 DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I SCREEN
K013628 DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I IGG/IGM TEST SYSTEM
K012450 DIAMEDIX IS-ANTI-CARDIOLIPIN IGA TEST SYSTEM
K012449 DIAMEDIX IS-ANTI-CARDIOLIPIN IGG/IGM TEST SYSTEM
K012795 DIAMEDIX IS-ANTI-GLIADIN IGG TEST SYSTEM
K012797 DIAMEDIX IS-ANTI-GLIADIN IGA TEST SYSTEM
K012053 DIAMEDIX IS-ANTI-CARDIOLIPIN SCREEN TEST SYSTEM
K002262 DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM
Search all 68 clearances from Diamedix Corp. →