• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name laser, comb, hair
510(k) Number K162994
Device Name Capillus302, Capillus312, Capillus352
Applicant
CAPILLUS, LLC
1715 NW 82nd AVE
miami,  FL  33126
Applicant Contact patricia schnoor
Correspondent
CAPILLUS, LLC
1715 NW 82nd AVE
miami,  FL  33126
Correspondent Contact patricia schnoor
Regulation Number890.5500
Classification Product Code
OAP  
Date Received10/27/2016
Decision Date 11/18/2016
Decision substantially equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel General & Plastic Surgery
summary summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-