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510k Database
Manufacturers
US
Biermar AG
Medical Device Manufacturer
·
US , Walker , MI
Biermar AG - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1982
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biermar AG
Radiology
✕
1
devices
1-1 of 1
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Cleared
Apr 23, 1982
MODEL PUP II AND MINI-NEBULIZER
K827291
Radiology
·
22d
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Radiology
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