Medical Device Manufacturer · US , Sisters , OR

Medisiss - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2003

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medisiss General & Plastic Surgery ✕

3 devices

1-3 of 3

Cleared Jul 23, 2010

MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01

General & Plastic Surgery · 148d

Cleared Aug 28, 2008

General & Plastic Surgery · 86d

Cleared Jan 23, 2004

MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS

General & Plastic Surgery · 332d