Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 Light Based Over-The-Counter Hair Removal
510(k) Number K183260
Device Name Sensilight Pro / Pistol IPL
Applicant
El Global Trade, Ltd.
8 Tzoran St., P.O.Box 8242
Netanya,  IL 4250608
Applicant Contact Shachar Raz
Correspondent
El Global Trade, Ltd.
8 Tzoran St., P.O.Box 8242
Netanya,  IL 4250608
Correspondent Contact Shachar Raz
Regulation Number878.4810
Classification Product Code
OHT  
Subsequent Product Code
ONF  
Date Received11/23/2018
Decision Date 03/18/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-