FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

THYROID MICROSOMAL ANTIGEN AUTO-ANTIBODY ENZYME

K Number: K930274 · Decision Feb 23, 1993
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
2
Review Days
35

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THYROID MICROSOMAL ANTIGEN AUTO-ANTIBODY ENZYME
K Number
K930274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Joldon Diagnostics
Date Received
January 19, 1993
Decision Date
February 23, 1993
Product Code
JZO
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
JZO System, Test, Thyroid Autoantibody

Similar 510(k) Clearances

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

View all

Other Clearances by Joldon Diagnostics

K Number Device Name
K925194 THYROGLOBULIN AUTO-ANTIBODY EIA TEST KIT