Company · IL

Bioview , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2014. 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
JOY	Device, Automated Cell-Locating	4
NTH	System, Automated Scanning Microscope And Image Analysis For Fluorescence In Situ Hybridization (Fish) Assays	1

Decided	510(k)	Device and applicant	Code
May 9, 2014	K130775	DUET SYSTEM Bioview , Ltd., IL	NTH
Jan 23, 2007	K061602	DUET SYSTEM Bioview , Ltd., IL	JOY
Aug 16, 2005	K050840	MODIFICATION TO DUET SYSTEM Bioview , Ltd., IL	JOY
Sep 16, 2004	K040591	DUET SYSTEM Bioview , Ltd., IL	JOY
Aug 20, 2003	K030192	DUET SYSTEM Bioview , Ltd., IL	JOY

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