FDA 510(k) Applications Submitted by KRIS SHAH

FDA 510(k) Number Submission Date Device Name Applicant
K010265 01/26/2001 BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265 BAYLIS MEDICAL CO., INC.
K990284 01/29/1999 BAYLIS MEDICAL RF SEPTOSTOMY GENERATOR, NYKANEN RF SEPTOSTOMY CATHETER, BAYLIS MEDICAL CONNECTOR CABLE BAYLIS MEDICAL CO., INC.
K020354 02/04/2002 BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL) BAYLIS MEDICAL CO., INC.
K031950 06/24/2003 BAYLIS PAIN MANAGEMENT GENERATOR, MODELS PMG-115-TD AND PMG-230-TD BAYLIS MEDICAL CO., INC.
K031951 06/24/2003 TRANSDISCAL SYSTEM (TRANSDISCAL PROBE), MODEL TDP-17-150-6 BAYLIS MEDICAL CO., INC.
K972846 08/01/1997 BMC RF CANNULA BAYLIS MEDICAL CO., INC.
K002389 08/04/2000 BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY BAYLIS MEDICAL CO., INC.
K002565 08/17/2000 BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE) BAYLIS MEDICAL CO., INC.
K013904 11/26/2001 BMC RADIO FREQUENCY PERFORATION GENERATOR, MODELS RFP-100-115 AND RFP-100-230 BAYLIS MEDICAL CO., INC.
K013919 11/27/2001 TORFLEX TRANSSEPTAL GUIDING SHEATH BAYLIS MEDICAL CO., INC.
K014075 12/11/2001 BMC COAXIAL INJECTABLE CATHETER, MODEL CIC 38/145 AND CIC 35/145 BAYLIS MEDICAL CO., INC.


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