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Suunto USA
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Medical Device Manufacturer
·
US , Carlsbad , CA
Suunto USA - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1997
Recent clearances:
CEBE
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Suunto USA
Ophthalmic
✕
1
devices
1-1 of 1
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Cleared
Jun 24, 1997
CEBE
K971644
·
HQY
Ophthalmic
·
50d
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Ophthalmic
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