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 Microscope, Surgical, General & Plastic Surgery
510(k) Number K926513
Device Name MOLLER-WEDEL OPERATING MICROSCOPE
Applicant
MOELLER MICROSURGICAL, INC.
40 WOODBRIDGE AVE.
METUCHEN,  NJ  08840
Applicant Contact RICHARD MONTGOMERY
Correspondent
MOELLER MICROSURGICAL, INC.
40 WOODBRIDGE AVE.
METUCHEN,  NJ  08840
Correspondent Contact RICHARD MONTGOMERY
Regulation Number878.4700
Classification Product Code
FSO  
Date Received12/30/1992
Decision Date 06/22/1993
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
-
-