• 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 Unit, Electrosurgical, And Accessories, Dental
510(k) Number K852522
Device Name SATALEC SERVOTOME
Applicant
Spelna, Inc.
P.O. Box 3395
Fredericksburg,  VA  22402
Applicant Contact ROBERT E MECDONNELL
Correspondent
Spelna, Inc.
P.O. Box 3395
Fredericksburg,  VA  22402
Correspondent Contact ROBERT E MECDONNELL
Regulation Number872.4920
Classification Product Code
EKZ  
Date Received06/14/1985
Decision Date 12/27/1985
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
-
-