Class Class II

UNIDRIVE SIII System (K223520)

K223520 2023-04-27 Traditional
Home/ Devices/ UNIDRIVE SIII System (K223520)

Description

UNIDRIVE SIII System by Karl Storz-Endoscopy-America, Inc. — FDA 510(k) cleared obstetrics/gynecology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223520
Clearance Date2023-04-27
Clearance TypeTraditional
Product CodeHIH
Regulation Number884.1690

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top