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Intercure , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020399RESPERATE; MODEL RR-150July 2, 2002
K000405INTERCURE LTD. RESPI-LOWMay 17, 2000