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 Epilator, High Frequency, Tweezer-Type
510(k) Number K972695
Device Name FINALLY FREE
Applicant
Mehl/Group Marketing
48 Mt. Olive Rd.
Budd Lake,  NJ  07828
Applicant Contact THOMAS BLAKE
Correspondent
Mehl/Group Marketing
48 Mt. Olive Rd.
Budd Lake,  NJ  07828
Correspondent Contact THOMAS BLAKE
Regulation Number878.5360
Classification Product Code
KCX  
Date Received07/18/1997
Decision Date 10/22/1997
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
-
-