• 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 Agent, Polishing, Abrasive, Oral Cavity
510(k) Number K771852
Device Name NIMETIC POLISHING PASTE
Applicant
Espe GmbH (Us)
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Espe GmbH (Us)
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number872.6030
Classification Product Code
EJR  
Date Received09/29/1977
Decision Date 11/02/1977
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
-
-