Versasae Plastic Cannula- 11 Gauge

• • Terminated Z-3030-2017 FDA Class II ·initiated 30 Jun 2017

  Punctures in blister packaging that was detected during the packaging process.

510(k) Number

K945070 ↗

FDA Product Code

FPA

Device Class

Class II

Regulation

21 CFR Part 880.5440

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K812035 Active Cleared 28 Jul 1981

See all devices from Imed Corp. →