FDA 510(k) Applications Submitted by OLDELFT CORP. OF AMERICA

FDA 510(k) Number Submission Date Device Name Applicant
K950037 01/04/1995 N 800 HF OLDELFT CORP. OF AMERICA
K892659 04/13/1989 ELECTRODELCA OLDELFT CORP. OF AMERICA
K912466 06/04/1991 OLDELFT SIMULIX-MC OLDELFT CORP. OF AMERICA
K923584 07/20/1992 THERAPAX DXT 300 SERIES 3 OLDELFT CORP. OF AMERICA
K914784 10/23/1991 PAPILLION PROCTOSCOPE OLDELFT CORP. OF AMERICA
K946128 12/15/1994 SIMULIX-HP OLDELFT CORP. OF AMERICA
K980296 01/27/1998 OLDELFT DIGIDELCA OLDELFT CORP. OF AMERICA
K973219 08/27/1997 AMBER DU OLDELFT CORP. OF AMERICA
K932848 06/10/1993 SIMULIX-MC CT EXTENSION OLDELFT CORP. OF AMERICA


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