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 Lamp, Endoscope, Incandescent
510(k) Number K914397
Device Name OXFORD OPTRONIX MPM 3S
Applicant
Dia-Stron, Ltd.
835-837 Sussex Blvd.
Broomall,  PA  19008
Applicant Contact MR. S RIMDZIUS
Correspondent
Dia-Stron, Ltd.
835-837 Sussex Blvd.
Broomall,  PA  19008
Correspondent Contact MR. S RIMDZIUS
Regulation Number876.1500
Classification Product Code
FTI  
Date Received10/01/1991
Decision Date 11/16/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-