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

KRONUS GLUTAMIC ACID DECARBOXYLASE ANTIBODY KIT

K Number: K051061 · Decision Nov 4, 2005
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
1
Applicant Total
11
Review Days
192

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Basic Information

Device Name
KRONUS GLUTAMIC ACID DECARBOXYLASE ANTIBODY KIT
K Number
K051061
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kronus Market Development Associates, Inc.
Date Received
April 26, 2005
Decision Date
November 4, 2005
Product Code
NWG
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
NWG Autoantibodies, Glutamic Acid Decarboxylase (Gad)

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Other Clearances by Kronus Market Development Associates, Inc.

K Number Device Name
DEN140001 ZINC TRANSPORTER 8 ANTIBODY (ZNT8AB) ELISA ASSAY KIT
K121046 STEROID 21-HYDROXYLASE ANTIBODY (21-OHAB) RIA ASSAY KIT
K111956 KRONUS VOLTAGE GATED CALCIUM CHANNEL (VGCC) ANTIBODY RIA ASSAY KIT
K080523 KRONUS BLOCKING ACETYLCHOLINE RECEPTOR AUTOANTIBODY (ACHRAB) RIA ASSAY KIT
K080159 KRONUS TSH RECEPTOR AUTOANTIBODY (TRAB) ELISA ASSAY KIT
K073590 KRONUS IA-2 AUTOANTIBODY RIA ASSAY KIT
K072135 KRONUS GAD AUTOANTIBODY ELISA ASSAY KIT
K070183 KRONUS INSULIN AUTOANTIBODY (IAA) ASSAY KIT
K042248 KRONUS, INC.'S ACETYLCHOLINE RECEPTOR ANTIBODY (ACHRAB) ASSAY KIT
K032134 TSH RECEPTOR ANTIBODY (TRAB) COATED TUBE (CT) ASSAY KIT
Search all 11 clearances from Kronus Market Development Associates, Inc. →