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 Orthosis, Cranial, Laser Scan
510(k) Number K203098
Device Name STARband, STARlight, St. Louis Band
Applicant
Orthomerica Products Inc.
6333 North Orange Blossom Trail
Orlando,  FL  32810
Applicant Contact David C. Kerr
Correspondent
Orthomerica Products Inc.
6333 North Orange Blossom Trail
Orlando,  FL  32810
Correspondent Contact Colton S. Carter
Regulation Number882.5970
Classification Product Code
OAN  
Subsequent Product Code
MVA  
Date Received10/14/2020
Decision Date 04/27/2021
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-