• 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
510(k) Number K851920
Device Name COMPRESSED AIR CONNECTOR DISPOSABLE CONNECTOR
Applicant
Dhd Medical Products Div. Diemolding Corp.
Division Of Diemolding Corp.
Canastota,  NY  13032
Applicant Contact JEAN WALLACE
Correspondent
Dhd Medical Products Div. Diemolding Corp.
Division Of Diemolding Corp.
Canastota,  NY  13032
Correspondent Contact JEAN WALLACE
Date Received05/02/1985
Decision Date 05/23/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-