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

CARDIOLIPIN IGA EIA TEST SYSTEM

K Number: K952522 · Decision Feb 9, 1996
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
93
Applicant Total
14
Review Days
253

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Basic Information

Device Name
CARDIOLIPIN IGA EIA TEST SYSTEM
K Number
K952522
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Immunoprobe, Inc.
Date Received
June 1, 1995
Decision Date
February 9, 1996
Product Code
MID
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
MID System, Test, Anticardiolipin Immunological

Similar 510(k) Clearances

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

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Other Clearances by Immunoprobe, Inc.

K Number Device Name
K972406 ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEM
K971393 MYCOPLASMA IGG ELISA TEST SYSTEM
K961765 MPO ELISA TEST SYSTEM
K961764 PR-3 ELISA TEST SYSTEM
K951549 EBNA IGG 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. →