• 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 hysteroscope (and accessories)
510(k) Number K191335
Device Name Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags
Applicant
Corinth MedTech, Inc.
1601 S. De Anza Blvd, Suite 200
cupertino,  CA  95014
Applicant Contact sandeep saboo
Correspondent
Corinth MedTech, Inc.
1601 S. De Anza Blvd, Suite 200
cupertino,  CA  95014
Correspondent Contact sandeep saboo
Regulation Number884.1690
Classification Product Code
HIH  
Subsequent Product Codes
GEI   HIG  
Date Received05/17/2019
Decision Date 06/06/2019
Decision substantially equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
summary summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-