FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

SHIELD ACTIVATED FACTOR XII (ELISA) ASSAY

K Number: K980885 · Decision Aug 21, 1998
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
27
Review Days
165

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Basic Information

Device Name
SHIELD ACTIVATED FACTOR XII (ELISA) ASSAY
K Number
K980885
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shield Diagnostics, Ltd.
Date Received
March 9, 1998
Decision Date
August 21, 1998
Product Code
GGP
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GGP Test, Qualitative And Quantitative Factor Deficiency

Similar 510(k) Clearances

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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
K972981 SHIELD HELICO-G2 ELISA KIT
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. →