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

ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM

K Number: K972406 · Decision Dec 22, 1997
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
10
Applicant Total
14
Review Days
179

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Basic Information

Device Name
ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM
K Number
K972406
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3020
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Immunoprobe, Inc.
Date Received
June 26, 1997
Decision Date
December 22, 1997
Product Code
GOD
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
GOD Antigens, Cf (Including Cf Control), Adenovirus 1-33

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Other Clearances by Immunoprobe, Inc.

K Number Device Name
K971393 MYCOPLASMA IGG ELISA TEST SYSTEM
K961765 MPO ELISA TEST SYSTEM
K961764 PR-3 ELISA TEST SYSTEM
K951549 EBNA IGG EIA TEST SYSTEM
K952522 CARDIOLIPIN IGA EIA TEST SYSTEM
K952523 CARDIOLIPIN IGG EIA TEST KIT
K952521 CARDIOLIPIN IGM EIA TEST SYSTEM
K951364 MICROSOMAL EIA TEST KIT
K951362 THYROGLOBULIN EIA TEST KIT
K951363 CARDIOLIPIN IGG,M,A EIA TEST SYSTEM
Search all 14 clearances from Immunoprobe, Inc. →