Capillus302, Capillus312, Capillus352— 510(k) K162994

Substantially Equivalent

Capillus, LLC

FDA 510(k) clearance K162994 for Capillus302, Capillus312, Capillus352, Substantially Equivalent on 2016-11-18. Applicant: Capillus, LLC. Device class: 2.

Clearance details

Applicant
Capillus, LLC
Product code
Code OAP
Device class
Class 2
Regulation
21 CFR 890.5500
Advisory panel
Physical Medicine
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Miami, FL, US
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