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 Stand, Infusion
510(k) Number K883260
Device Name DITTMAR POWER LIFTER
Applicant
Dittmar and Penn Corp.
101 E. Laurel Ave.
P.O. Box 66
Cheltenham,  PA  19012
Applicant Contact J. J NOWAK
Correspondent
Dittmar and Penn Corp.
101 E. Laurel Ave.
P.O. Box 66
Cheltenham,  PA  19012
Correspondent Contact J. J NOWAK
Regulation Number880.6990
Classification Product Code
FOX  
Date Received08/03/1988
Decision Date 11/07/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-