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

DIAMEDIX IS-HSV 1 & 2 IGG TEST SYSTEM

K Number: K981306 · Decision Sep 29, 1998
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
37
Applicant Total
68
Review Days
172

Basic Information

Device Name
DIAMEDIX IS-HSV 1 & 2 IGG TEST SYSTEM
K Number
K981306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DIAMEDIX CORP.
Date Received
April 10, 1998
Decision Date
September 29, 1998
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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