A-M Systems, Inc.

A-M Systems, Inc. holds 2 FDA 510(k) medical device clearances, first cleared 2000, most recent 2007, with 1 FDA device recall on record.

FDA recalls by A-M Systems, Inc.

Z-0120-2019 — Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer. This tubing is supplied non-sterile P/N: 1024920 Rev. 01 Low temperature smooth interior tubing is a disposable pulmonary equipment interconnect used in ventilation and aesthesia machines.Class II·Terminated·2018-08-10

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by A-M Systems, Inc.

K063526 — A-M SYSTEMS VIROMAX VIRAL AND BACTERIAL FILTERCode CAH·2007-06-29
K000654 — VBMAXCode CAH·2000-11-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.

Top product codes for A-M Systems, Inc.

FDA recalls by A-M Systems, Inc.

Recent clearances by A-M Systems, Inc.