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510(k) K791645

Device
VICKERS MEDICAL MODEL 112 TREONIC DC2
Applicant
VICKERS AMERICA MEDICAL CORP.
510(k) number
K791645
Product code
FKW  
Decision
Substantially Equivalent (SESE)
Decision date
1979-10-02
Date received
1979-08-23
Regulation
876.5540
Classification name
Tip, Vessel
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FKW  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K893438T SERIES VESSEL TIPSAkcess Medical Products, Inc.1989-06-08
K810257VESSEL TIPS, SIZES 13-18Quinton, Inc.1981-03-13

Legacy Summary#

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FDA Review#

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