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 K040055
Device Name POLYLASE LP
Applicant
DDC TECHNOLOGIES, INC.
2980 WAVERLY AVE.
OCEANSIDE,  NY  11572
Applicant Contact DMITRY DONSKOY
Correspondent
DDC TECHNOLOGIES, INC.
2980 WAVERLY AVE.
OCEANSIDE,  NY  11572
Correspondent Contact DMITRY DONSKOY
Regulation Number878.4810
Classification Product Code
GEX  
Date Received01/12/2004
Decision Date 04/07/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-