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

PREMIER HSV PLUS

K Number: K953839 · Decision May 23, 1996
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
37
Applicant Total
92
Review Days
281

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Basic Information

Device Name
PREMIER HSV PLUS
K Number
K953839
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meridian Diagnostics, Inc.
Date Received
August 16, 1995
Decision Date
May 23, 1996
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LGC), ordered by most recent decision date.

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Other Clearances by Meridian Diagnostics, Inc.

K Number Device Name
K993914 PREMIER TOXINS A&B, MODEL 616096
K990263 IMMUNOCARD STAT! E. COLI O157:H7
K984346 PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TEST
K984343 PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST
K983255 MODIFICATION TO: PREMIER PLATINUM HPSA
K982764 PREMIER CRYPTOSPORIDIUM
K982711 PREMIER GIARDIA
K980076 PREMIER PLATINUM HPSA
K980077 PARA-PAK SPINCON
K971585 IMMUNOCARD STAT! ROTAVIRUS
Search all 92 clearances from Meridian Diagnostics, Inc. →