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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.
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