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

CALCIUM CHLORIDE SOLUTION 0.1M, IN HEPES BUFFER

K Number: K880302 · Decision Feb 19, 1988
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
98
Applicant Total
15
Review Days
25

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Basic Information

Device Name
CALCIUM CHLORIDE SOLUTION 0.1M, IN HEPES BUFFER
K Number
K880302
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Hemotec, Inc.
Date Received
January 25, 1988
Decision Date
February 19, 1988
Product Code
GGN
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
GGN Plasma, Coagulation Control

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Other Clearances by Hemotec, Inc.

K Number Device Name
K902081 CLOTTRAC(TM) IBEX HEPARINASE HR ACT CART./CONTROL
K894359 CLOTRAC CITRATED WHOLE BLOOD COAGULATION CONTROLS
K894317 HEMOTEC HEPCON HMS COAGULATION SYSTEM & ACCESS.
K894466 HEPCON(R) CV WHOLE BLOOD COAGULATION CONTROLS
K884590 HEPCON/SYSTEM B-10 HEPARIN ASSAY/SCREEN/CARTRIDGES
K875089 HEPCON SYSTEM B-10 ACTIVATED CLOT TIME & HEPARIN
K854377 HEMOTEC CV WHOLE BLOOD COAGULATION CONTROLS
K854376 HEMOTEC CITRATED WHOLE BLOOD COAGULATION CONTROLS
K853789 ADDITIONAL HEMOTEC HEPCON/SYS B-10 COAGULATION CAR
K843459 HEMOTEC ACT I SYSTEM
Search all 15 clearances from Hemotec, Inc. →