Medical Device Manufacturer · GB , Cheshire Wa 15 8ah

Sabre-K , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Recent clearances: KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOC

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sabre-K , Ltd. Dental ✕

1 devices

1-1 of 1

Cleared Sep 30, 1998

KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4...