Steritec Products Mfg. (A Getinge Group Company) - FDA 510(k) Cleared...
1
Total
1
Cleared
0
Denied
Steritec Products Mfg. (A Getinge Group Company) has 1 FDA 510(k) cleared medical devices. Based in Engelwood, US.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Steritec Products Mfg. (A Getinge Group Company) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Getinge as regulatory consultant.
1 devices