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
510(k) Number K837216
Device Name MODEL XA-15 LASER SYSTEM FOR SURGERY
Applicant
Xanar, Inc.
2868 Janitell Rd.
Colorado Springs,  CO  80906
Correspondent
Xanar, Inc.
2868 Janitell Rd.
Colorado Springs,  CO  80906
Date Received02/28/1983
Decision Date 04/04/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-