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 Scaler, Ultrasonic
510(k) Number K880940
Device Name AMDENT MODEL 830 ULTRASONIC SCALER
Applicant
Pathway Products, Inc.
6800 Westgate 139b-148
Austin,  TX  78745
Applicant Contact LEE W PALMER
Correspondent
Pathway Products, Inc.
6800 Westgate 139b-148
Austin,  TX  78745
Correspondent Contact LEE W PALMER
Regulation Number872.4850
Classification Product Code
ELC  
Date Received03/07/1988
Decision Date 07/15/1988
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
-
-