Scanlan Intl., Inc.
Scanlan Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1996.
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.