FDA 510(k) Applications Submitted by JAMES R WHITNEY

FDA 510(k) Number Submission Date Device Name Applicant
K980870 03/04/1998 RUSCH SILICONE FOLEY CATHETER RUSCH, INC.
K981203 04/02/1998 RUSCH BLAKEMORE 3 LUMEN, STERILE RUSCH INTL.
K971643 05/05/1997 RUSCH BRILLANT BALLOON CATHETER RUSCH INTL.
K972184 06/10/1997 RUSCH BRILLANT SILICONE FOLEY CATHETER RUSCH INTL.
K972423 06/27/1997 RUSCH TRACHEOFIX-SET RUSCH INTL.
K972546 07/08/1997 RUSCH SINGLE USE CRYSTAL TRACHEOSTOMY TUBE SET RUSCH INTL.
K983125 09/08/1998 EPIDURAL CATHETER MODELS 1210/1200 RUSCH INTL.
K973892 10/14/1997 RUSCH BLAKEMORE TUBE - 4 LUMEN (MINNESOTA TYPE) RUSCH INTL.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact