Skip to content
Scan

Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K092864

AESPIRE 7900, AESPIRE VIEW · Datex-Ohmeda Inc., A Division of Instrumentarium C · decided 2010-01-12 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Aespire7900DATEX-OHMEDA INCBSZ00840682102261