FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

SHIELD HELICO-G2 ELISA KIT

K Number: K972981 · Decision Mar 17, 1998
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
27
Review Days
218

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Basic Information

Device Name
SHIELD HELICO-G2 ELISA KIT
K Number
K972981
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3110
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shield Diagnostics, Ltd.
Date Received
August 11, 1997
Decision Date
March 17, 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 Shield Diagnostics, Ltd.

K Number Device Name
K000398 SHIELD VON WILLEBRAND FACTOR ACTIVITY ELISA, MODEL FVWF 200
K982879 SHIELD DIASTAT ANTI-B2 GLYCOPROTEIN 1 IGG (ELISA) ASSAY
K980885 SHIELD ACTIVATED FACTOR XII (ELISA) ASSAY
K962825 SHIELD VON WILLEBRAND FACTOR ACTIVITY (ELISA) ASSAY
K963525 DIASTAT ANTI-GLOMERULAR BASEMENT MEMBRANE KIT
K961515 QUANTASE PHENYLALANINE ASSAY
K955303 DIASTAT ANTI-CARDIOLIPIN KIT
K952183 DIASTAT ANTI-THYROGLOBULIN KIT
K951487 DIASTAT ANTI-THYROID PEROXIDASE KIT
K943630 DIASTAT ANTI-MPO (PANCA) KIT
Search all 27 clearances from Shield Diagnostics, Ltd. →