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FDA 510(k) Applications Submitted by BRUCE R LESTER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050343
02/11/2005
REPROCESSED HARMONIC SCALPELS
STERILMED, INC.
K041127
04/30/2004
MODIFICATION TO: REPROCESSED OXIMAX PULSE OXIMETER SENSORS
STERILMED, INC.
K042648
09/28/2004
REPROCESSED COLD BIOPSY FORCEPS
STERILMED, INC.
K043453
12/15/2004
STERILEMED REPROCESSED IVUS IMAGING CATHETER
STERILMED, INC.
K050136
01/21/2005
REPROCESSED HOT BIOPSY FORCEPS
STERILMED, INC.
K051220
05/12/2005
REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS
STERILMED, INC.
K053188
11/15/2005
REPROCESSED BALOON INFLATION DEVICE
STERILMED, INC.
K043513
12/20/2004
STERILMED REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETER
STERILMED, INC.
K043592
12/29/2004
REPROCESSED ENDOSCOPIC TROCAR
STERILMED, INC.
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