Medical Device Manufacturer · US , Washington , DC

Intercure , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Recent clearances: RESPERATE, INTERCURE LTD. RESPI-LOW

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Intercure , Ltd. Neurology ✕

2 devices

1-2 of 2

Cleared Jul 02, 2002

Neurology · 146d

Cleared May 17, 2000

INTERCURE LTD. RESPI-LOW

Neurology · 100d