• 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 rfid chip for dental appliance
510(k) Number K170423
Device Name DentureID Microchip
Applicant
CMP Industries LLC
413 N. Pearl St.
albany,  NY  12207
Applicant Contact devon o. howe
Correspondent
CMP Industries LLC
413 N. Pearl St.
albany,  NY  12207
Correspondent Contact devon o. howe
Regulation Number880.6300
Classification Product Code
PYQ  
Date Received02/13/2017
Decision Date 10/25/2017
Decision substantially equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-