Thomas Medical Products, Inc.
FDA 510(k) medical device clearances.
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.