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

IMX HOMOCYSTEINE

K Number: K980812 · Decision Oct 1, 1998
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
42
Applicant Total
3
Review Days
212

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Basic Information

Device Name
IMX HOMOCYSTEINE
K Number
K980812
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5600
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Axis Biochemicals, Asa
Date Received
March 3, 1998
Decision Date
October 1, 1998
Product Code
DFC
Advisory Committee
Immunology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
DFC Lipoprotein, Low-Density, Antigen, Antiserum, Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DFC), ordered by most recent decision date.

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Other Clearances by Axis Biochemicals, Asa

K Number Device Name
K992274 MODIFICATION TO IMX HOMOCYSTEINE
K980907 AXIS HOMOCYSTEINE ENZYME IMMUNOASSAY