Aries Medical, Inc.
FDA 510(k) medical device clearances.
Top product codes for Aries Medical, Inc.
Recent clearances by Aries Medical, Inc.
- K912604 — SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIF
- K903925 — ARIES MELDICAL MODEL 2100HC HANK CRANK
- K903442 — ARIES TAPERSEAL(TM) SHEATH
- K895433 — ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYS
- K882289 — ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.
- K864537 — 40CC PERCUTANEOUS PRE-FURL (D/L) BALLOON CATHETER
- K864994 — 40CC PER. PRE-FURL (S/L) INTRA-AORTIC CATHETER
- K864567 — 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
- K864568 — 40CC SURGICAL DOUBLE LUMEN BALLOON CATHETER
- K871140 — ARIES PEEL AWAY PERCUTANEOUS CATHETER INTRODUCER
- K870189 — ARIES TAPERED SHEATH
- K863185 — 40CC PERCUTANEOUS FURL SINGLE INTRA-AORTIC BALLOON
- K844220 — ARIES MEDICAL PERFLEX PERCUTANEOUS 40CC D/L BALLOO
- K850111 — AIRES TUOHY NEEDLES 17GA. X 4 1/2
- K842004 — PERCUTANEOUS CATHETER INTRODUCER SET
- K833632 — ARIES MEDICAL MODEL 700
- K840201 — EPIDURAL CATHETER TRAY
- K840202 — EPIDURAL CATHETER
- K840641 — VESSEL DILATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.