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

SYSING AND HEMOGLOBIN REAGENT

K Number: K780829 · Decision Jun 22, 1978
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
38
Applicant Total
116
Review Days
34

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Basic Information

Device Name
SYSING AND HEMOGLOBIN REAGENT
K Number
K780829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5620
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Harleco
Date Received
May 19, 1978
Decision Date
June 22, 1978
Product Code
GKR
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GKR System, Hemoglobin, Automated

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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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