• 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 device, electrical dental anesthesia
510(k) Number K935085
Device Name 3M DENTAL ELECTRONONIC ANESTHESIA (DEA0 SYSTEM 8670 ADDITIONAL APPLICATIONS
Applicant
3M COMPANY
3M CENTER
BLDG. 275-3SE-08
ST. PAUL,  MN  55144 -1000
Applicant Contact PAUL A BURGIO
Correspondent
3M COMPANY
3M CENTER
BLDG. 275-3SE-08
ST. PAUL,  MN  55144 -1000
Correspondent Contact PAUL A BURGIO
Classification Product Code
LWM  
Date Received10/22/1993
Decision Date 01/26/1994
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-