Baylis Medical Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: SUREFLEX STEERABLE GUIDING SHEATH KIT, OSTEOCOOL (TM) RF ABLATION SYSTEM, TORFLEX TRANSSEPTAL GUIDING SHEATH
28
Total
28
Cleared
0
Denied
FDA 510(k) Regulatory Record - Baylis Medical Co., Inc. General Hospital ✕
1 devices