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

BIOTEL MICROALBUMINURIA (TM)

K Number: K894169 · Decision Sep 18, 1989
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
37
Applicant Total
39
Review Days
95

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Basic Information

Device Name
BIOTEL MICROALBUMINURIA (TM)
K Number
K894169
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1645
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Diagnostic Corp.
Date Received
June 15, 1989
Decision Date
September 18, 1989
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.)

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K962655 ANEROID AND MERCURIAL SPHYGMOMANOMETERS
K940686 ELECTRONIC THERMOMETERS
K935944 PROSCOPES AND ADSCOPES
K932145 COAGULATION REFERENCE PLASMA, NORMAL
K893608 ACTICHROME ATIII KIT
K884941 ACTICLOT C KIT
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