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

KODAK SURECELL HERPES (HSV) CONTROL FLUID SET

K Number: K903926 · Decision Sep 17, 1990
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
37
Applicant Total
238
Review Days
27

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Basic Information

Device Name
KODAK SURECELL HERPES (HSV) CONTROL FLUID SET
K Number
K903926
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Eastman Kodak Company
Date Received
August 21, 1990
Decision Date
September 17, 1990
Product Code
LGC
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
LGC Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific

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