Millar Nonmagnectic Mikro-Tip Catheter Press. Tran

FDA 510(k) K915775 · Millar Instruments, Inc.

Substantially Equivalent

510(k) numberK915775

Submission

Device name
Millar Nonmagnectic Mikro-Tip Catheter Press. Tran
Applicant
Millar Instruments, Inc.
Houston, TX, US
Received
December 24, 1991
Decision date
April 20, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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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
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
K860766Millar Pulsed Doppler VelocimeterDPW · Traditional 07/29/1986SE

Questions and answers

When was Millar Nonmagnectic Mikro-Tip Catheter Press. Tran cleared by the FDA?

Millar Nonmagnectic Mikro-Tip Catheter Press. Tran (K915775) received a 510(k) decision of Substantially Equivalent on April 20, 1992, 118 days after the submission was received.

What is the product code of K915775?

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