FDA 510(k), K163170, Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352
FDA 510(k), K163170, Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352
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510(K) Number: K163170
Device Name: Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352
Manufacturer: CAPILLUS, LLC
Device Classification Name: laser, comb, hair
Regulation Number: 890.5500
Classification Product Code: OAP
Date Received: 11/14/2016
Decision Date: 01/31/2017
Regulation Medical Specialty: Physical Medicine
Device Name: Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352
Manufacturer: CAPILLUS, LLC
Device Classification Name: laser, comb, hair
Regulation Number: 890.5500
Classification Product Code: OAP
Date Received: 11/14/2016
Decision Date: 01/31/2017
Regulation Medical Specialty: Physical Medicine
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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