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

AUTO TOTAL PROTEIN

K Number: K761217 · Decision Dec 21, 1976
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
115
Applicant Total
116
Review Days
14

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Basic Information

Device Name
AUTO TOTAL PROTEIN
K Number
K761217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1635
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Harleco
Date Received
December 7, 1976
Decision Date
December 21, 1976
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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K813039 ULTRACHEM E-CHOL, ITEM #65025
K813043 ULTRACHEM CREA ITEM #64972
K813040 ULTRACHEM CA, ITEM #64975
K813044 ULTRACHEM ALB, ITEM #64970
K813041 ULTRAZYME-GT, ITEM #64959 & 65032
K813038 ULTRACHEM TP, ITEM #64974
K812593 ULTRA ZYME PLUS CK-1 #64978, 65027 & 28
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