Aktiebolaget Leo Diagnostics

Aktiebolaget Leo Diagnostics holds 1 FDA 510(k) medical device clearance, cleared in 1983.

Top product codes for Aktiebolaget Leo Diagnostics

GKR — Hematology1 device

Recent clearances by Aktiebolaget Leo Diagnostics

K832020 — HEMOCUE PHOTOMETER TECHNICAL MANUALCode GKR·1983-10-28

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