FDA 510(k), K140190, NIGHT SHIFT
FDA 510(k), K140190, NIGHT SHIFT
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$149.00 USD
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510(K) Number: K140190
Device Name: NIGHT SHIFT
Manufacturer: ADRIENNE LENZ
Device Classification Name: Pillow, Cervical (For Mild Sleep Apnea)
Regulation Number: MYB
Classification Product Code: 01/24/2014
Date Received: 05/29/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ear Nose & Throat
Device Name: NIGHT SHIFT
Manufacturer: ADRIENNE LENZ
Device Classification Name: Pillow, Cervical (For Mild Sleep Apnea)
Regulation Number: MYB
Classification Product Code: 01/24/2014
Date Received: 05/29/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ear Nose & Throat