510(k) K230159

Device
SoundBite® Crossing System XS Peripheral
Applicant
Soundbite Medical Solutions, Inc.
510(k) number
K230159
Product code
PDU
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-28
Date received
2023-01-19
Regulation
870.1250
Classification name
Catheter For Crossing Total Occlusions
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Diane Marceau
Address
2300 Alfred Nobel, Suite 230 Montreal CA H4S 2A4 H4S 2A4

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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