Baylis Medical Co., Inc.
Baylis Medical Co., Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2013.
Top product codes for Baylis Medical Co., Inc.
Recent clearances by Baylis Medical Co., Inc.
- K122926 — SUREFLEX STEERABLE GUIDING SHEATH KIT
- K111523 — OSTEOCOOL (TM) RF ABLATION SYSTEM
- K102948 — TORFLEX TRANSSEPTAL GUIDING SHEATH
- K102192 — INDISCAL DIGITAL MANOMETER
- K101372 — DUOCOOL PAIN MANAGEMENT PROBE, MODEL OSP-17-180-20
- K101615 — POWERWIRE RADIOFREQUENCY GUIDEWIRE
- K101117 — LEV-OR DILATION CATHETER OTW
- K092877 — INDISCAL ASPIRATION DEVICE AND ACCESSORIES
- K092337 — PAIN MANAGEMENT OPTIMA, MODEL PMO21-100-05, PMO20-100-10CS, PMO20-145-10CS
- K073326 — NRG TRANSSEPTAL NEEDLE
- K072478 — BAYLIS PAIN MANAGEMENT GENERATOR-TD, MODELS: PMG-115-TD AND PMG-230-TD
- K071745 — BAYLIS PAIN MANAGEMENT SINGLE-USE PROBE
- K062937 — TRANSDISCAL SYSTEM, MODELS TDP-17-150-6, TDI-17-150, TDA-PPU-1, TDA-TBK-1, TDX-Y-TSW-TDP, TDX-PMG-PPU
- K051670 — RF TUNNELER WIRE
- K053082 — BAYLIS PAIN MANAGEMENT COOLED PROBE, MODEL PMPC-18-150-6
- K031949 — TORONTO RF SEPTOSTOMY CATHETER, MODEL TSC-50-75
- K031951 — TRANSDISCAL SYSTEM (TRANSDISCAL PROBE), MODEL TDP-17-150-6
- K031950 — BAYLIS PAIN MANAGEMENT GENERATOR, MODELS PMG-115-TD AND PMG-230-TD
- K023334 — BMC CATHETER CONNECTOR CABLE, MODEL RFP-101
- K020354 — BAYLIS PAIN MANAGEMENT GENERATOR (PMG), MODELS PMG-115 (DOMESTIC), PMG-230 (INTERNATIONAL)
- K014075 — BMC COAXIAL INJECTABLE CATHETER, MODEL CIC 38/145 AND CIC 35/145
- K013919 — TORFLEX TRANSSEPTAL GUIDING SHEATH
- K013904 — BMC RADIO FREQUENCY PERFORATION GENERATOR, MODELS RFP-100-115 AND RFP-100-230
- K002565 — BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE)
- K010265 — BAYLIS MEDICAL RF PERFORATION PROBE, MODEL RFP-265
- K990284 — BAYLIS MEDICAL RF SEPTOSTOMY GENERATOR, NYKANEN RF SEPTOSTOMY CATHETER, BAYLIS MEDICAL CONNECTOR CABLE
- K002389 — BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY
- K972846 — BMC RF CANNULA
Data sourced from openFDA. This site is unofficial and independent of the FDA.