Innersense Disposable Microtransducer

FDA 510(k) K941283 · Becton Dickinson Vascular Access, Inc.

Substantially Equivalent

510(k) numberK941283

Submission

Device name
Innersense Disposable Microtransducer
Applicant
Becton Dickinson Vascular Access, Inc.
Sandy, UT, US
Received
March 17, 1994
Decision date
April 19, 1994
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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Questions and answers

When was Innersense Disposable Microtransducer cleared by the FDA?

Innersense Disposable Microtransducer (K941283) received a 510(k) decision of Substantially Equivalent on April 19, 1994, 33 days after the submission was received.

What is the product code of K941283?

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