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, Needle-Type
510(k) Number K893389
Device Name MODEL SE-5 EPILATOR
Applicant
R. A. FISCHER CO. CORP.
517 COMMERCIAL ST.
GLENDALE,  CA  91203
Applicant Contact VAN ORDEN
Correspondent
R. A. FISCHER CO. CORP.
517 COMMERCIAL ST.
GLENDALE,  CA  91203
Correspondent Contact VAN ORDEN
Regulation Number878.5350
Classification Product Code
KCW  
Date Received05/01/1989
Decision Date 06/05/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-