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 Powered Laser Surgical Instrument
510(k) Number K020673
Device Name WAVE FORM MANUFACTURING PROLASE GENERAL SHAPED FIBER
Applicant
Wave Form Mfg., Inc.
8317 Front Beach Rd.
Suite 21
Panama City Beach,  FL  32407
Applicant Contact JOE D BROWN
Correspondent
Wave Form Mfg., Inc.
8317 Front Beach Rd.
Suite 21
Panama City Beach,  FL  32407
Correspondent Contact JOE D BROWN
Regulation Number878.4810
Classification Product Code
GEX  
Date Received03/01/2002
Decision Date 05/30/2002
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
-
-