Transducer-Monitor Interfacing

FDA 510(k) K842150 · Millar Instruments, Inc.

Substantially Equivalent

510(k) numberK842150

Submission

Device name
Transducer-Monitor Interfacing
Applicant
Millar Instruments, Inc.
Houston, TX, US
Received
May 30, 1984
Decision date
October 26, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXO – Transducer, Pressure, Catheter Tip
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2870
Specialty
Cardiovascular

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More from Edwards Lifeciences, LLC

510(k)DeviceDecision
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K013205Millar Pressure Control Unit Model PCU-2000DRQ · Traditional 07/02/2002SE
K993694Mikro-Tip Angiographic CatheterDQO · Special 03/01/2000SE
K952773Mikro-Tip Angiographic CatheterDQO · Traditional 11/07/1995SE
K935166Flow Directed Mikro-Tip Pressure TransducerDXO · Traditional 08/05/1994SE
K915775Millar Nonmagnectic Mikro-Tip Catheter Press. TranDXO · Traditional 04/20/1992SE
K896264Millar Mikro-Tip Doppler CatheterJOP · Traditional 01/24/1990SE
K895721Millar Mikro-Tip Pulse TransducerDXO · Traditional 12/07/1989SE
K883651Millar Mikro-Tip Catheter Pressure TransducerDQO · Traditional 11/18/1988SE

Questions and answers

When was Transducer-Monitor Interfacing cleared by the FDA?

Transducer-Monitor Interfacing (K842150) received a 510(k) decision of Substantially Equivalent on October 26, 1984, 149 days after the submission was received.

What is the product code of K842150?

The FDA product code is DXO – Transducer, Pressure, Catheter Tip, a Class II (moderate risk) device regulated under 21 CFR 870.2870.