Bentley-Trantec Dispos. Domes D-260-

FDA 510(k) K841811 · American Bentley

Substantially Equivalent

510(k) numberK841811

Submission

Device name
Bentley-Trantec Dispos. Domes D-260-
Applicant
American Bentley
Mchenry, IL, US
Received
May 1, 1984
Decision date
September 9, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DRS – Transducer, Blood-Pressure, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2850
Specialty
Cardiovascular

Other 510(k)s with product code DRS

510(k)DeviceApplicantDecision
K254074TruPressDRS · Traditional Procerus Enterprises09/10/2026SE
K242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensorsDRS · Special Edwards Lifesciences, LLC03/21/2025SE
K221782Meritrans ECO Reusable Pressure Transducer, Meritrans ECO DomesDRS · Traditional Merit Medical Pte. , Ltd.03/17/2023SE
K172458HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus…DRS · Traditional Smiths Medical Asd, Inc.11/09/2017SE
K163172HemoDraw Plus Closed Blood Sampling System with LogiCal Transducer Kit, HemoDraw Plus…DRS · Traditional Smiths Medical Asd, Inc.05/24/2017SE
K161408Compass Cast and MAPDRS · Traditional Centurion Medical Products Corporation11/22/2016SE
K152472Disposable Pressure TransducerDRS · Traditional Zhejiang Haisheng Medical Device Co., Ltd.10/31/2016SE
K152980Flo Trac sensor, Volume View sensorDRS · Traditional Edwards Lifesciences, LLC01/19/2016SE
K151040Art-line Single channel blood pressure system, Art-line Double channel blood pressure…DRS · Traditional Biometrix , Ltd.09/04/2015SE
K133624Compass CT, Compass CT PortDRS · Traditional Mirador Biomedical04/18/2014SE

More from Mirador Biomedical

510(k)DeviceDecision
K872896Umbilical Artery Oxygen Probe Model UAP-100CCE · Traditional 02/12/1988SE
K873923Integrated Membrane Oxygenator W/Cardiotomy FilterDTZ · Traditional 11/06/1987SE
K872167Cardiotomy/Mediastinal Auto. Reservoir CATR-3500DTP · Traditional 09/01/1987SE
K870804Cardioplegia Heat Exchanger Model No. HE-100DTR · Traditional 09/01/1987SE
K872133Oxygenator Model No. Bentley 5 PlusDTZ · Traditional 08/24/1987SE
K870911Indwelling Blood Carbondioxide Partial Pres. AnalyCCC · Traditional 05/29/1987SE
K870269Electrosurgical Meniscus Cutter (Emc) Mod. AMC-100GEI · Traditional 03/09/1987SE
K863249Oxygenator Model No. BENTLEY-10 PlusDTZ · Traditional 10/20/1986SE
K861641Heparin-Coated Extracorporeal CircuitsDTZ · Traditional 09/29/1986SE
K862549Arterial Blood Filter Holder Model No. Af-HeKRI · Traditional 07/15/1986SE

Questions and answers

When was Bentley-Trantec Dispos. Domes D-260- cleared by the FDA?

Bentley-Trantec Dispos. Domes D-260- (K841811) received a 510(k) decision of Substantially Equivalent on September 9, 1985, 496 days after the submission was received.

What is the product code of K841811?

The FDA product code is DRS – Transducer, Blood-Pressure, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2850.