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FDA 510(k) Applications Submitted by JULIE A BEAUMONT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990547
02/22/1999
PILLING WECK SURGICAL Y STENT FORCEPS
PILLING WECK, INC.
K010797
03/16/2001
RUSCH MILLER-ABBOTT TUBE
RUSCH INTL.
K010798
03/16/2001
RUSCH CANTOR TUBE
RUSCH INTL.
K011121
04/12/2001
RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS
RUSCH INTL.
K011122
04/12/2001
BALLPEN SPINAL NEEDLE W/WO INTRODUCER
RUSCH INTL.
K011210
04/19/2001
THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMY
RUSCH INTL.
K991647
05/13/1999
TFX MEDICAL INTRODUCER KIT
TFX MEDICAL GROUP
K992664
08/09/1999
TFX MEDICAL STYLET CATHETER
TFX MEDICAL GROUP
K993063
09/13/1999
RUSCH BRILLANT SILICONE FOLEY
RUSCH INTL.
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