• 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 Cleanser, Denture, Over The Counter
510(k) Number K925259
Device Name CFR MONOGRAPH
Applicant
Combe, Inc.
1101 Westchester Ave.
White Plains,  NY  10604
Applicant Contact DANIEL R JOHNSON
Correspondent
Combe, Inc.
1101 Westchester Ave.
White Plains,  NY  10604
Correspondent Contact DANIEL R JOHNSON
Regulation Number872.3520
Classification Product Code
EFT  
Date Received10/19/1992
Decision Date 01/11/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-