Sensi-Touch Combo Spinal/Epidural Regional Anesthesia Delivery System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K962880 ↗

FDA Product Code

CAZ

Device Class

Class II

Regulation

21 CFR Part 868.5140

Advisory Committee

Anesthesiology

FDA Decision

SESK Substantially Equivalent — Kit

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See all devices from Sherwood Medical Co. →