Medical Device Manufacturer · US , Denver , CO

Voco GmbH - FDA 510(k) Cleared Devices

117 submissions · 117 cleared · Since 1991

117

Total

117

Cleared

0

Denied

117 devices

76-100 of 117

Cleared Jun 28, 2005

MODIFICATION TO:REGISTRADO X-TRA

Cleared Nov 01, 2004

Cleared Oct 20, 2004

IONOFIL PLUS AC

Cleared Apr 07, 2004

Cleared Nov 25, 2003

Cleared Oct 31, 2003

IONOFIL COLOR AC

Cleared Jun 19, 2003

Cleared Jun 13, 2003

FINAL VARNISH LC

Cleared May 30, 2003

Cleared May 30, 2003

Cleared Oct 10, 2002

Cleared Aug 14, 2002

REGISTRADO X-TRA

Cleared Jul 29, 2002

Cleared Jul 19, 2002

Cleared Mar 06, 2002

Cleared Jul 18, 2001

Cleared Nov 15, 2000

Cleared Feb 07, 2000

Cleared Feb 03, 2000

Cleared Jan 20, 2000

Cleared Jan 12, 2000

Cleared Mar 23, 1998

Cleared Feb 10, 1998

Cleared Apr 13, 1994

Cleared Jun 17, 1993

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