Company · US

Voss Medical Products

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1993. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
DWF	Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass	1
DXC	Clamp, Vascular	1
FQO	Table, Operating-Room, Ac-Powered	1
KIL	Positioner, Socket	1
KPK	Marker, Ostia, Aorto-Saphenous Vein	1

Decided	510(k)	Device and applicant	Code
Jun 1, 1993	K932187	PRONE POSITIONER Voss Medical Products	KIL
Jun 1, 1993	K932186	BYPASS LEG POSITIONER Voss Medical Products	FQO
May 17, 1990	K896338	VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA Voss Medical Products	DWF
Dec 22, 1989	K885161	VOSS VEIN CLAMP Voss Medical Products	DXC
Sep 27, 1989	K895369	VOSS GRAFT MARKER Voss Medical Products	KPK

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.