• 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 tester, color vision
510(k) Number K844694
Device Name TITMUS VISION TESTER II
Applicant
TITMUS OPTICAL, INC.
PETERSBURG,  VA  23803
Applicant Contact KINSEY
Correspondent
TITMUS OPTICAL, INC.
PETERSBURG,  VA  23803
Correspondent Contact KINSEY
Regulation Number886.1170
Classification Product Code
HIT  
Date Received12/03/1984
Decision Date 01/22/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-