Weinmann Gerate Fur Medizin GmbH + Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Weinmann Gerate Fur Medizin GmbH + Co. KG - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Weinmann Gerate Fur Medizin GmbH + Co. KG has 9 FDA 510(k) cleared medical devices. Based in Hamburg, DE.
Historical record: 9 cleared submissions from 2006 to 2011. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Weinmann Gerate Fur Medizin GmbH + Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Weinmann Gerate Fur Medizin GmbH + Co. KG
9 devices
Cleared
Nov 16, 2011
SOYALA SILKGEL FULL FACE MASK
Anesthesiology
111d
Cleared
Jul 12, 2011
EASYFIT SILKGEL NASAL MASK
Anesthesiology
104d
Cleared
Mar 11, 2011
NP15
Anesthesiology
190d
Cleared
May 09, 2008
SOYALA GEL VENTED
Anesthesiology
30d
Cleared
Mar 28, 2008
SOYALA FULL FACE MASK GEL VENTED
Anesthesiology
92d
Cleared
Dec 14, 2007
WEINMANNCOMPACT, MODEL WM 27380
Anesthesiology
144d
Cleared
Jul 18, 2007
WEINMANNCOMFORT 2, MODEL WM 27600 AND WEINMANNAQUA, MODEL WM 27603
Anesthesiology
83d
Cleared
Nov 09, 2006
SOYALA FULL FACE MASK
Anesthesiology
149d
Cleared
Jun 21, 2006
SOYALA, SOYALA BLUE
Anesthesiology
125d