Lock-It Plus Regional Anesthesia Catheter Securement Device, Model 100/399/216

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K051524 ↗

FDA Product Code

BSO

Models / Variants

100

399

216

Device Class

Class II

Regulation

21 CFR Part 868.5120

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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