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

LUMI-AGGREGOMETER

K Number: K771198 · Decision Aug 2, 1977
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
16
Review Days
32

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Basic Information

Device Name
LUMI-AGGREGOMETER
K Number
K771198
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6675
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Chrono-Log Corp.
Date Received
July 1, 1977
Decision Date
August 2, 1977
Product Code
JBY
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
JBY Aggregometer, Platelet, Photo-Optical Scanning

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JBY), ordered by most recent decision date.

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Other Clearances by Chrono-Log Corp.

K Number Device Name
K161329 Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channel
K050265 CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700
K032951 CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592A
K962426 CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592
K945414 RISTOCETIN COFACTOR ASSAY KIT
K940792 AGGRO/LINK VW COFACTOR SOFTWARE
K932566 AGGRO/LINK CONTROL SOFTWARE
K922800 PLATELET AGGREGATION REAGENTS
K851025 AGGRO/LINK COMPUTER INTERFACE
K850592 PLATELET AGGREGATION REAGENT
Search all 16 clearances from Chrono-Log Corp. →