Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO holds 4 FDA 510(k) medical device clearances, first cleared 1998, most recent 2013.

Top product codes for Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

Recent clearances by Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

K132102 — BECE CAD ZIRKON HT+Code EIH·2013-11-12
K123929 — BEGOPAL+Code EJH·2013-03-14
K090434 — BECE PRESSCode EIH·2009-07-06
K983081 — BEGOPAL 300Code EJS·1998-10-28

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