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 Sunglasses (Non-Prescription Including Photosensitive)
510(k) Number K951131
Device Name SUNGLASSES, NONPRESCRIPTION
Applicant
Gold, Inc.
4999 Oakland St.
Denver,  CO  80239
Applicant Contact WILLIAM GOLD III
Correspondent
Gold, Inc.
4999 Oakland St.
Denver,  CO  80239
Correspondent Contact WILLIAM GOLD III
Regulation Number886.5850
Classification Product Code
HQY  
Date Received03/13/1995
Decision Date 05/10/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-