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

CARDIOLIPIN A EIA TEST SYSTEM

K Number: K946216 · Decision Jan 24, 1996
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
93
Applicant Total
26
Review Days
399

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Basic Information

Device Name
CARDIOLIPIN A EIA TEST SYSTEM
K Number
K946216
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hogan & Hartson
Date Received
December 21, 1994
Decision Date
January 24, 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

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Other Clearances by Hogan & Hartson

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K950169 RIBOSOMAL P EIA TEST SYSTEM
K942389 TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES
K946217 CARDIOLIPIN M EIA TEST SYSTEM
K946215 CARDIOLIPIN G EIA TEST SYSTEM
K946186 CHAL-2500
K941566 COMPUSPEAK
K950110 MARDX MITOCHONDRIA EIA TEST SYSTEM
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