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

MDI GLIADIN A TEST

K Number: K002358 · Decision Oct 19, 2000
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
41
Applicant Total
11
Review Days
78

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Basic Information

Device Name
MDI GLIADIN A TEST
K Number
K002358
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5750
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micro Detect, Inc.
Date Received
August 2, 2000
Decision Date
October 19, 2000
Product Code
MST
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
MST Antibodies, Gliadin

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Other Clearances by Micro Detect, Inc.

K Number Device Name
K003794 ELISA TEST, SEROLOGY
K002359 MDI GLIADIN G TEST
K000934 MDI SCL-70 TEST
K000477 MDI DS-DNA TEST
K994029 MDI SM TEST
K993843 MDI RF TEST
K993971 MDI SS-B TEST ENZYME IMMUNOASSAY FOR THE DETECTION OF AUTOANTIBODIES TO SS-B IN HUMAN SERUM
K993636 MDI SS-A TEST
K993635 MDI SM/RNP TEST
K973508 PYLORI DETECT IGG
Search all 11 clearances from Micro Detect, Inc. →