Separation Technology, Inc.

Separation Technology, Inc. holds 2 FDA 510(k) medical device clearances, first cleared 1989, most recent 1991, with 1 FDA device recall on record.

FDA recalls by Separation Technology, Inc.

Z-1367-2013 — SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells onto a glass slide from any fluid suspension.Class II·Terminated·2013-03-13

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 Separation Technology, Inc.

K913128 — HEMATASTAT C-70BCode GKG·1991-09-23
K890849 — HEMATASTAT H-70Code GKG·1989-03-21

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

Top product codes for Separation Technology, Inc.

FDA recalls by Separation Technology, Inc.

Recent clearances by Separation Technology, Inc.