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Rusch Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
43
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K033023INTERMITTENT URETHRAL CATHETERSDecember 23, 2003
K030559RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEMJune 30, 2003
K023666RUSCH GUIDED CHOLANGIOGRAPHY CATHETERJune 17, 2003
K023918RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESSMarch 28, 2003
K023964RUSCH MICROLARYNGEAL TUBEDecember 23, 2002
K021540RUSCH EDGAR TUBEAugust 1, 2002
K021764RUSCH TRACHEOFIX SET, CUFFED AND UNCUFFEDJuly 23, 2002
K020714RUSCH FLONEIL; FLOCATH INTROGELJuly 1, 2002
K010797RUSCH MILLER-ABBOTT TUBEFebruary 26, 2002
K010798RUSCH CANTOR TUBEFebruary 26, 2002
K013872RUSCH MEMORY BAGFebruary 12, 2002
K013266RUSCH POLYFLEX STENT KITNovember 27, 2001
K010596RUSCH BRONCHUS BLOCKER KITNovember 21, 2001
K011121RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETSNovember 16, 2001
K011122BALLPEN SPINAL NEEDLE W/WO INTRODUCERNovember 16, 2001
K011210THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMYAugust 15, 2001
K010068RUSCH POLYFLEX STENT FOR THE ESOPHAGUS WITH INTRODUCER SYSTEMFebruary 8, 2001
K000070FLOCATHFebruary 18, 2000
K993786RUSCH ORAL/NASAL (SAFETY CLEAR PLUS) TRACHEAL TUBE CUFFED, MAGILL/MURPHYFebruary 2, 2000
K993063RUSCH BRILLANT SILICONE FOLEYDecember 9, 1999