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 Laser, Surgical, Gynecologic
510(k) Number K872352
Device Name FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA
Applicant
LASER MEDIA
77 ARKAY DR.
HAUPPAUGE,  NY  11788
Applicant Contact ROBERT A KAPLAN
Correspondent
LASER MEDIA
77 ARKAY DR.
HAUPPAUGE,  NY  11788
Correspondent Contact ROBERT A KAPLAN
Regulation Number884.4550
Classification Product Code
HHR  
Date Received06/17/1987
Decision Date 12/30/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-