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 K854134
Device Name FIBEROPTIC COLLIMATING HANDPIECE
Applicant
Dawn Laser Technology, Inc.
718 Willowglen Rd.
Santa Barbara,  CA  93105
Applicant Contact NYLE G UTTERBACK
Correspondent
Dawn Laser Technology, Inc.
718 Willowglen Rd.
Santa Barbara,  CA  93105
Correspondent Contact NYLE G UTTERBACK
Regulation Number878.4810
Classification Product Code
GEX  
Date Received10/10/1985
Decision Date 02/07/1986
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
Predetermined Change
Control Plan Authorized		 No
-
-