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 spectacle, magnifying
510(k) Number K820732
Device Name LA VEL LATERAL VIEW EXTENSION LENS
Applicant
PETER M. TOLLIVER
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
PETER M. TOLLIVER
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number886.5840
Classification Product Code
HOI  
Date Received03/17/1982
Decision Date 05/03/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-