FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

IMMUNOCARD MYCOPLASMA

K Number: K934550 · Decision Sep 20, 1994
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
12
Applicant Total
92
Review Days
363

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Basic Information

Device Name
IMMUNOCARD MYCOPLASMA
K Number
K934550
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3375
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meridian Diagnostics, Inc.
Date Received
September 22, 1993
Decision Date
September 20, 1994
Product Code
LJZ
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
LJZ Enzyme Linked Immunoabsorbent Assay, Mycoplasma Spp.

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. →