Thomas Medical Products, Inc.
Thomas Medical Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2013.
Top product codes for Thomas Medical Products, Inc.
Recent clearances by Thomas Medical Products, Inc.
- K122431 — HEARTSPAN STEERABLE INTRODUCER KIT
- K120158 — CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITS
- K101015 — GUIDE CATHETERS AND ACCESSORIES
- K083269 — CROSSOVER
- K081341 — REINFORCED CATHETER INTRODUCER SYSTEM (RCIS)
- K072745 — Y-GLIDE
- K043438 — LARGE BORE SPLITTABLE INTRODUCER KIT
- K040713 — MODIFICATION TO BRAIDED GUIDING INTRODUCER SYSTEM
- K011727 — TRANSSEPTAL NEEDLE/TROCAR
- K020090 — MODIFICATION TO TRANSSEPTAL INTRODUCER SET
- K013202 — MODIFICATION TO BRAIDED GUIDING INTRODUCER
- K004025 — SPLITTABLE SHEATH INTRODUCER KIT
- K004026 — BRAIDED GUIDING INTRODUCER
- K003731 — SAFESHEATH MSP INTRODUCER SHEATH KIT WITH INTEGRAL HEMOSTASIS VALVE
- K961780 — HEMODIALYSIS INTRODUCER SET
- K961466 — PERCUTANEOUS INTRODUCER SET
- K934901 — TEAR-AWAY SHEATH INTRODUCER SET WITH INTEGRAL HEMOSTASIS VALVE
- K931587 — MULTI-PORT Y INTRODUCER SET
- K932619 — TRANSSEPTAL INTRODUCER SET
- K924456 — LONG LENGTH PERCUTANEOUS INTRODUCER SET
- K911130 — HEMOSTATIC Y CONNECTOR
- K904608 — PERCUTANEOUS INTRODUCER TRAY
- K902275 — PERCUTANEOUS INTRODUCER SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.