Apheresis Technologies, Inc.

Apheresis Technologies, Inc. holds 2 FDA 510(k) medical device clearances, first cleared 1993, most recent 1996, with 1 FDA device recall on record.

FDA recalls by Apheresis Technologies, Inc.

Z-2149-2012 — Plasma Pump Model PP-04a Used with Asahi Plasmaflo Plasma Separators and plasma exchange tubesets to perform therapeutic plasma exchange.Class II·Terminated·2012-07-09

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 Apheresis Technologies, Inc.

K961137 — ATI PLASMA PUMP (PP-04)Code FIR·1996-06-14
K926409 — PLASMA DISCARD BAGSCode LKN·1993-03-02

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

Top product codes for Apheresis Technologies, Inc.

FDA recalls by Apheresis Technologies, Inc.

Recent clearances by Apheresis Technologies, Inc.