Inovo, Inc. Accupulse Single Lumen Conserving Regulator

FDA 510(k) K060751 · Inovo, Inc.

Substantially Equivalent

510(k) numberK060751

Submission

Device name
Inovo, Inc. Accupulse Single Lumen Conserving Regulator
Applicant
Inovo, Inc.
Naples, FL, US
Received
March 21, 2006
Decision date
July 18, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NFB – Conserver, Oxygen
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5905
Specialty
Anesthesiology

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More from Chad Therapeutics, Inc.

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K141967Purefill Oxygen CompressorCAW · Traditional 11/07/2014SE
K113111Chad Therapeutic Evolution Electronic Oxygen Conserver with MotionNFB · Special 12/08/2011SE
K103392Chad Therapeutic Evolution Electronic Oxygen ConserverNFB · Special 12/17/2010SE
K051540Inovo, Inc. Independence Oxygen Conserving RegulatorNFB · Traditional 09/21/2005SE
K031983Inovo, Inc, Economizer Conserving RegulatorNFB · Traditional 09/15/2003SE

Questions and answers

When was Inovo, Inc. Accupulse Single Lumen Conserving Regulator cleared by the FDA?

Inovo, Inc. Accupulse Single Lumen Conserving Regulator (K060751) received a 510(k) decision of Substantially Equivalent on July 18, 2006, 119 days after the submission was received.

What is the product code of K060751?

The FDA product code is NFB – Conserver, Oxygen, a Class II (moderate risk) device regulated under 21 CFR 868.5905.