510(k) K980898

Device
FEMOSTOP II DISPOSABLE SET, FEMOSTOP II COMPRESSION ARCH, FEMOSTOP II PUMP, FEMOSTOP II BILATERAL ADAPTER
Applicant
RADI MEDICAL SYSTEMS AB
510(k) number
K980898
Product code
DXC  
Decision
Substantially Equivalent (SESE)
Decision date
1998-04-21
Date received
1998-03-09
Regulation
870.4450
Classification name
Clamp, Vascular
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
MATS GRANLUND
Address
Palmbladsgatan 10 Uppsala SE S-754 50 S-754 50

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code DXC  #

510(k), Device, Applicant table
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K230281PICOCLAMPKono Seisakusho Co., Ltd.2023-10-23
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K230248VIOLAVascular Graft Solutions, Ltd.2023-02-28
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K221843GEM Biover Microvascular ClampsSynovis Micro Companies Alliance, Inc.2022-09-14
K213531TR BAND Radial Compression DeviceTerumo Medical Corporation2021-12-20
K210681SiteSeal SVEnsite Vascular2021-04-06
K210324V. Mueller Cosgrove Flex Clamps, Model Number-CV1033, CV1061, CV1133, CV1161, CV1186Carefusion 2200, Inc.2021-03-04
K210006MI DeTACHBiorep Technologies, Inc.2021-03-04
K203307VIOLAVascular Graft Solutions, Ltd.2021-02-17

Legacy Summary#

summary

FDA Review#

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