510(k) K230603

Device
Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19); Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19); Arrow Stimulating SnapLock
Applicant
Teleflex Medical
510(k) number
K230603
Product code
BSO
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-30
Date received
2023-03-03
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
Kristen Bisanz
Address
3015 Carrington Mill Blvd. Morrisville NC US 27560 27560

FDA Registration Numbers

Source Documents

510(k) summary PDF

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