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Arrow Non-Stimulating SnapLock Adapter (K-05520-005C) +4 more models

FDA 510(k)

Class II (US FDA 510(k))

510(k) K230603

by Teleflex Medical

Identifiers

510(k) Number
K230603 FDA 510(k)
FDA Product Code
BSO FDA 510(k)
Models / Variants
Arrow Non-Stimulating SnapLock Adapter (K-05520-005C) FDA 510(k)
Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19) FDA 510(k)
Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19) FDA 510(k)
Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001) FDA 510(k)
Arrow Stimulating SnapLock Adapter (with tab) (TZ-05000-002) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 868.5120 FDA 510(k)
Regulation Number
868.5120 FDA 510(k)
Advisory Committee
Anesthesiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Arrow Non-Stimulating SnapLock Adapter (K-05520-005C) +4 more models by Teleflex Medical — Class II — FDA_510K — listed in FDA 510(k) — 5 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Teleflex Medical

Sources (1)

  • FDA 510(k) K230603 24 fields · synced Jun 19, 2026