Medical Device Manufacturer · US , Nederland , CO

Spacelabs Healthcare, Ltd. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2011

Recent clearances: Eclipse MINI Model 98900, Eclipse PRO, Spacelabs Lifescreen PRO Analyzer

9
Total
9
Cleared
0
Denied

Spacelabs Healthcare, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Nederland, US.

Last cleared in 2022. Active since 2011. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Spacelabs Healthcare, Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Speed TO Market, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Spacelabs Healthcare, Ltd.

9 devices
1-9 of 9
Filters