Scanlan Intl., Inc.
FDA 510(k) medical device clearances.
Top product codes for Scanlan Intl., Inc.
Recent clearances by Scanlan Intl., Inc.
- K960372 — SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM
- K945474 — SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER
- K911184 — SCANLAN/TAHERI VALVULOTOME
- K864919 — SCANLAN (TM) VEIN/GRAFT HOLDER
- K864920 — SCANLAN (TM) INSTRUMENT TRAY
- K851825 — SCANLAN TUNNELER, SHEATH & TIP
- K841521 — SCANLAN ENDARSECTOR
- K841513 — SCANLAN ATRAUM INSTRUMENT JAW COVER
- K841085 — SCANLAN COLORMARK SKIN MARKER
- K841514 — SCANLAN VASCU-STATT II APPROXIMATOR
- K841515 — SCANLAN VASCU-STATT II
- K841086 — SURGICAL INSTRUMENT DEMAGNETIZER
- K823764 — SCANLAN SINGLE-USE AORTA PUNCH
- K823694 — VASCU-STATT APPROXIMATOR
- K821887 — SCANLAN SUTURE-STATT
- K810480 — SCANLAN SUTURE BOOTS
- K802829 — SCANLAN VASCU-STATT
- K801976 — SCANLAN STERNUM NEEDLE-SUTURE
- K780255 — NEEDLE DRIVER
Data sourced from openFDA. This site is unofficial and independent of the FDA.