Medical Device Manufacturer · US , Great Neck , NY

Inovo, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2003
6
Total
6
Cleared
0
Denied

Inovo, Inc. has 6 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 6 cleared submissions from 2003 to 2014. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Inovo, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Inovo, Inc.
6 devices
1-6 of 6
Cleared Nov 07, 2014
PUREFILL OXYGEN COMPRESSOR
K141967 · CAW
Anesthesiology · 109d
Cleared Dec 08, 2011
CHAD THERAPEUTIC EVOLUTION ELECTRONIC OXYGEN CONSERVER WITH MOTION
K113111 · NFB
Anesthesiology · 49d
Cleared Dec 17, 2010
CHAD THERAPEUTIC EVOLUTION ELECTRONIC OXYGEN CONSERVER
K103392 · NFB
Anesthesiology · 28d
Cleared Jul 18, 2006
INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR
K060751 · NFB
Anesthesiology · 119d
Cleared Sep 21, 2005
INOVO, INC. INDEPENDENCE OXYGEN CONSERVING REGULATOR
K051540 · NFB
Anesthesiology · 103d
Cleared Sep 15, 2003
INOVO, INC, ECONOMIZER CONSERVING REGULATOR
K031983 · NFB
Anesthesiology · 81d
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