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

N-ASSAY TIA MICROALBUMIN

K Number: K934146 · Decision Jan 11, 1994
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
37
Applicant Total
29
Review Days
140

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Basic Information

Device Name
N-ASSAY TIA MICROALBUMIN
K Number
K934146
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1645
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Crestat Diagnostics, Inc.
Date Received
August 24, 1993
Decision Date
January 11, 1994
Product Code
JIR
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JIR), 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. →