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

CONTROL, HEMATOLOGY, CH-60

K Number: K781077 · Decision Jul 27, 1978
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
191
Applicant Total
44
Review Days
29

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Basic Information

Device Name
CONTROL, HEMATOLOGY, CH-60
K Number
K781077
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.8625
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Dade, Baxter Travenol Diagnostics, Inc.
Date Received
June 28, 1978
Decision Date
July 27, 1978
Product Code
JPK
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
JPK Mixture, Hematology Quality Control

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Other Clearances by Dade, Baxter Travenol Diagnostics, Inc.

K Number Device Name
K800296 WHOLE BLOOD GAS CONTROL, LEVELS 1,2,&3
K792606 WHOLE BLOOD PLATELET CONTROL NORMAL,
K792723 BLOOD FLUID FILTERS
K792607 T3 UPTAKE (T3U) REAGENTS
K792443 TSH RADIOIMMUNOASSAY
K792442 FERRITIN RADIOIMMUNOASSAY
K791922 HARLECO BRAND CLINICARD LIPASE TEST SET
K792183 DADE HIGH DENSITY LIPOPROTEIN CHOLESTERO
K790767 IMMU-TEK AUTOMATIC CENTRIFUGE
K790776 DADE LOW IONIC STRENGTH SOLUITION (LISS)
Search all 44 clearances from Dade, Baxter Travenol Diagnostics, Inc. →