Accutron, Inc.

Accutron, Inc. holds 5 FDA 510(k) medical device clearances, first cleared 1997, most recent 2005, with 4 FDA device recalls on record.

Top product codes for Accutron, Inc.

FDA recalls by Accutron, Inc.

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 Accutron, Inc.

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