Aries Medical, Inc.
Aries Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1991.
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.