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

IMMUNOCARD MONO

K Number: K930778 · Decision Dec 27, 1993
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
58
Applicant Total
92
Review Days
314

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Basic Information

Device Name
IMMUNOCARD MONO
K Number
K930778
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5640
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meridian Diagnostics, Inc.
Date Received
February 16, 1993
Decision Date
December 27, 1993
Product Code
KTN
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
KTN System, Test, Infectious Mononucleosis

Similar 510(k) Clearances

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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. →