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

NOVA TOTAL PROTEIN MODULE

K Number: K923266 · Decision Aug 12, 1992
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
115
Applicant Total
89
Review Days
41

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Basic Information

Device Name
NOVA TOTAL PROTEIN MODULE
K Number
K923266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1635
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nova Biomedical Corp.
Date Received
July 2, 1992
Decision Date
August 12, 1992
Product Code
CEK
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
CEK Biuret (Colorimetric), Total Protein

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K091547 NOVA MAX PLUS BLOOD GLUCOSE AND B-KETONE MONITOR SYSTEM, NOVA MAX PLUS B-KETONE CONTROL SOLUTIONS, NOVA MAX BLOOD GLUCOS
K070960 NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEM
K070255 NOVA MAX BLOOD GLUCOSE MONITOR SYSTEM, 90001,90002
K070068 NOVA STATSENSOR CREATININE HOSPITAL METER, CONTROL SOLUTIONS,LINEARITY SOLUTIONS, AND TEST STRIPS
K063821 NOVA STATSTRIP GLUCOSE HOSPITAL METER SYSTEM
K061830 STAT PROFILE CRITICAL CARE XPRESS (CCX), MODEL 1+
K060345 NOVA STATSTRIP GLUCOSE HOSPITAL METER, STATSTRIP CONTROL SOLUTIONS
K041016 NOVA GLUCOSE LOW/HIGH LEVEL CONTROL SOLUTIONS
Search all 89 clearances from Nova Biomedical Corp. →