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

CHOLINESTERASE TEST KIT

K Number: K912148 · Decision Aug 12, 1991
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
25
Applicant Total
29
Review Days
89

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Basic Information

Device Name
CHOLINESTERASE TEST KIT
K Number
K912148
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3240
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Crestat Diagnostics, Inc.
Date Received
May 15, 1991
Decision Date
August 12, 1991
Product Code
DIH
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DIH Colorimetry, Cholinesterase

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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. →