Arrow Non-Stimulating SnapLock Adapter - Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001)

FDA 510(k)

Class II (US FDA 510(k))

510(k) K230603

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 - Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001) by Teleflex Medical — Class II — FDA_510K — listed in…

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Source	Region	Type	Cert / Approval No.	Class	Status
FDA 510(k)	United States	FDA_510K	K230603	Class II	Active

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Manufacturer

Manufacturer: Teleflex Medical

Sources (1)

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