Save-Simplified Automated Ventilator, Models: 550X10, 600X10 and 600X12

FDA 510(k) K071221 · Automedx, Inc.

Substantially Equivalent

510(k) numberK071221

Submission

Device name
Save-Simplified Automated Ventilator, Models: 550X10, 600X10 and 600X12
Applicant
Automedx, Inc.
Germantown, MD, US
Received
May 2, 2007
Decision date
September 6, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTL – Ventilator, Emergency, Powered (Resuscitator)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5925
Specialty
Anesthesiology
Life-sustaining
Yes

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K221634Oxymag - Transport and Emergency VentilatorBTL · Traditional Magnamed Tecnologia Medica S/A05/24/2023SE
K202219VORTRAN GO2VENT with PEEP ValveBTL · Traditional Vortran Medical Technology 1, Inc.02/11/2021SE
K193191MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagBTL · Traditional Weinmann Emergency Medical Technology GmbH + Co.…11/20/2020SE
K182956Puffin Lite Infant Resuscitation SystemBTL · Special International Biomedical01/18/2019SE
K173373SafeT T-Piece ResuscitatorBTL · Traditional Ventlab, LLC11/16/2018SE
K161420Moves SLCBTL · Traditional Thornhill Research, Inc.06/06/2017SE
K162968Vortran GO2VENTBTL · Traditional Vortran Medical Technology 1, Inc.04/10/2017SE
K141595O-Two E700,O-TWO E600,O-TWO E500BTL · Traditional O-Two Medical Technologies, Inc.03/16/2015SE
K142096T-Piece ResuscitatorBTL · Traditional Mercury Medical10/17/2014SE

More from Mercury Medical

510(k)DeviceDecision
K131877Save II, Save II BasicBTL · Traditional 03/21/2014SE

Questions and answers

When was Save-Simplified Automated Ventilator, Models: 550X10, 600X10 and 600X12 cleared by the FDA?

Save-Simplified Automated Ventilator, Models: 550X10, 600X10 and 600X12 (K071221) received a 510(k) decision of Substantially Equivalent on September 6, 2007, 127 days after the submission was received.

What is the product code of K071221?

The FDA product code is BTL – Ventilator, Emergency, Powered (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5925.