• 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 perimeter, automatic, ac-powered
510(k) Number K902878
Device Name MT-336 AUTOMATIC PERIMETER
Applicant
MARCO TECHNOLOGIES
R.D. #3 BOX 237
WELISEWITZ ROAD
RINGOES,  NJ  08551
Applicant Contact RANDOLPH L COOKE
Correspondent
MARCO TECHNOLOGIES
R.D. #3 BOX 237
WELISEWITZ ROAD
RINGOES,  NJ  08551
Correspondent Contact RANDOLPH L COOKE
Regulation Number886.1605
Classification Product Code
HPT  
Date Received07/02/1990
Decision Date 09/18/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-