510(k) BK190321

Device
Automated Blood Grouping And Antibody Test Systems
Applicant
Diagnostic Grifols, S. A.
510(k) number
BK190321
Product code
KSZ  
Decision
Substantially Equivalent (SE)
Decision date
2019-12-10
Date received
2019-02-12
Regulation
864.9175
Classification name
System, Test, Automated Blood Grouping And Antibody
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Clearance type
510(k) Special
Third party reviewed
No

Other 510(k) Records For Product Code KSZ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K810899TECHNICON AUTOGROUPER 16-C SYSTEMTechnicon Instruments Corp.1981-05-05
K790282ELDONCARDNordisk Infuser System1979-05-04
K771098BLOOD GROUPING SYS., BG-9Technicon Instruments Corp.1977-08-04
K770185RH CONTROL DILUENTBd Becton Dickinson Vacutainer Systems Preanalytic1977-03-14

Legacy Summary#

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FDA Review#

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