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

PREMIER PLATINUM HPSA

K Number: K980076 · Decision May 12, 1998
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
92
Review Days
124

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Basic Information

Device Name
PREMIER PLATINUM HPSA
K Number
K980076
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meridian Diagnostics, Inc.
Date Received
January 8, 1998
Decision Date
May 12, 1998
Product Code
LYR
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
LYR Helicobacter Pylori

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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
K980077 PARA-PAK SPINCON
K971585 IMMUNOCARD STAT! ROTAVIRUS
K961508 IMMUNOCARD H. PYLORI
Search all 92 clearances from Meridian Diagnostics, Inc. →