Medical Vision AB

Medical Vision AB holds 1 FDA 510(k) medical device clearance, cleared in 2010, with 1 FDA device recall on record.

FDA recalls by Medical Vision AB

Z-2705-2016 — Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures.Class II·Terminated·2016-05-10

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 Medical Vision AB

K093409 — POWERPUMP ARTHROSCOPY SYSTEMCode HRX·2010-02-24

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

Top product codes for Medical Vision AB

FDA recalls by Medical Vision AB

Recent clearances by Medical Vision AB