510(k) K221655

Device
Multiflex Steerable Sheath
Applicant
Vizaramed, Inc.
510(k) number
K221655
Product code
DYB
Decision
Substantially Equivalent (SESE)
Decision date
2022-11-14
Date received
2022-06-07
Regulation
870.1340
Classification name
Introducer, Catheter
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Jack P Douglas
Address
1914 O'Toole Way San Jose CA US 95131 95131

FDA Registration Numbers

Source Documents

510(k) summary PDF

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