510(k) K231242

Device
Perifix FX Catheter; Contiplex FX Catheter
Applicant
B.Braun Medical, Inc.
510(k) number
K231242
Product code
BSO
Decision
Substantially Equivalent (SESE)
Decision date
2023-09-15
Date received
2023-05-01
Regulation
868.5120
Classification name
Catheter, Conduction, Anesthetic
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Tracy Larish
Address
3773 Corporate Pkwy. Center Valley PA US 18034 18034

FDA Registration Numbers

Source Documents

510(k) summary PDF

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