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

N-ASSAY TIA TRANSFERRIN TEST KIT

K Number: K964295 · Decision Jun 16, 1997
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
29
Review Days
230

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Basic Information

Device Name
N-ASSAY TIA TRANSFERRIN TEST KIT
K Number
K964295
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5880
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Crestat Diagnostics, Inc.
Date Received
October 29, 1996
Decision Date
June 16, 1997
Product Code
DDG
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
DDG Transferrin, Antigen, Antiserum, Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DDG), ordered by most recent decision date.

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Other Clearances by Crestat Diagnostics, Inc.

K Number Device Name
K980883 N-ASSAY GLU-UL
K981276 N-ASSAY L D-BIL
K981289 N-ASSAY L T-BIL
K980902 N-ASSAY L AST/GOT
K980900 N-ASSAY CPK-L
K971985 N-ASSAY TIA PLASMINOGEN TEST KIT
K972257 N-ASSAY TIA ANTITHROMBIN III TEST KIT
K964296 N-ASSAY TIA APO B TEST KIT
K964294 N-ASSAY TIA APO A1/B MULTI CALIBRATOR
K964292 N-ASSAY TIA APO A1 TEST KIT
Search all 29 clearances from Crestat Diagnostics, Inc. →