FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

LACRYTEST

K Number: K034057 · Decision Mar 9, 2004
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
1
Review Days
70

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Basic Information

Device Name
LACRYTEST
K Number
K034057
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Adiatec SA
Date Received
December 30, 2003
Decision Date
March 9, 2004
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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