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 K921320
Device Name ELIOS DIODE OPHTHALMIC LASER
Applicant
Marco Ophthalmic, Inc.
11825 Central Pkwy.
Jacksonville,  FL  32224
Applicant Contact SCOTT E LEWIS
Correspondent
Marco Ophthalmic, Inc.
11825 Central Pkwy.
Jacksonville,  FL  32224
Correspondent Contact SCOTT E LEWIS
Regulation Number878.4810
Classification Product Code
GEX  
Date Received03/19/1992
Decision Date 07/02/1992
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
-
-