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510k Database
Manufacturers
US
Intercure , Ltd.
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Medical Device Manufacturer
·
US , Washington , DC
Intercure , Ltd. - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 2000
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Intercure , Ltd.
Neurology
✕
2
devices
1-2 of 2
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Cleared
Jul 02, 2002
RESPERATE
K020399
·
HCC
Neurology
·
146d
Cleared
May 17, 2000
INTERCURE LTD. RESPI-LOW
K000405
·
HCC
Neurology
·
100d
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Neurology
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