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 System, X-Ray, Extraoral Source, Digital
510(k) Number K220277
Device Name Digital Intraoral X-ray Sensor
Applicant
Shenzhen Xpectvision Technology Co., Ltd.
B507,Block A And B,Nanshan Medical Device Industrial Park,
Nanhai Ave. 1019,Nanshan District
Shenzhen,  CN 518067
Applicant Contact Mengsi Peng
Correspondent
Shenzhen Xpectvision Technology Co., Ltd.
B507,Block A And B,Nanshan Medical Device Industrial Park,
Nanhai Ave. 1019,Nanshan District
Shenzhen,  CN 518067
Correspondent Contact Mengsi Peng
Regulation Number872.1800
Classification Product Code
MUH  
Date Received01/31/2022
Decision Date 02/17/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-