FDA 510(k), K150572, Respire Pink Series-Herbst-EF
FDA 510(k), K150572, Respire Pink Series-Herbst-EF
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$149.00 USD
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$149.00 USD
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510(K) Number: K150572
Device Name: Respire Pink Series-Herbst-EF
Manufacturer: Respire Medical Holding
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 03/06/2015
Decision Date: 08/27/2015
Regulation Medical Specialty: Dental
Device Name: Respire Pink Series-Herbst-EF
Manufacturer: Respire Medical Holding
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 03/06/2015
Decision Date: 08/27/2015
Regulation Medical Specialty: Dental