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

COBAS(R) CORE IGE TOTAL EIA

K Number: K930890 · Decision Aug 5, 1993
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
296
Review Days
164

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Basic Information

Device Name
COBAS(R) CORE IGE TOTAL EIA
K Number
K930890
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Roche Diagnostic Systems, Inc.
Date Received
February 22, 1993
Decision Date
August 5, 1993
Product Code
DGC
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
DGC Ige, Antigen, Antiserum, Control

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