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 Agent, Tooth Bonding, Resin
510(k) Number K141839
Device Name PREMIER ETCH
Applicant
PREMIER DENTAL PRODUCTS CO.
1710 ROMANO DR.
PLYMOUTH MEETING,  PA  19462
Applicant Contact VINCENT D'ALESSANDRO
Correspondent
PREMIER DENTAL PRODUCTS CO.
1710 ROMANO DR.
PLYMOUTH MEETING,  PA  19462
Correspondent Contact VINCENT D'ALESSANDRO
Regulation Number872.3200
Classification Product Code
KLE  
Date Received07/08/2014
Decision Date 11/17/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-