• 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 System, Imaging, Pulsed Echo, Ultrasonic
510(k) Number K920906
Device Name DGH-500 PACHYMETER
Applicant
Dgh Technology, Inc.
446 Lancaster Ave.
Frazer,  PA  19355
Applicant Contact LUTHER DETWEILER
Correspondent
Dgh Technology, Inc.
446 Lancaster Ave.
Frazer,  PA  19355
Correspondent Contact LUTHER DETWEILER
Regulation Number892.1560
Classification Product Code
IYO  
Date Received02/27/1992
Decision Date 11/02/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-