Innovision Audio

FDA 510(k) K193218 · Innovere Medical, Inc.

Substantially Equivalent

510(k) numberK193218

Submission

Device name
Innovision Audio
Applicant
Innovere Medical, Inc.
Markham, CA
Received
November 21, 2019
Decision date
April 7, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LNH – System, Nuclear Magnetic Resonance Imaging
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1000
Specialty
Radiology

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Questions and answers

When was Innovision Audio cleared by the FDA?

Innovision Audio (K193218) received a 510(k) decision of Substantially Equivalent on April 7, 2020, 138 days after the submission was received.

What is the product code of K193218?

The FDA product code is LNH – System, Nuclear Magnetic Resonance Imaging, a Class II (moderate risk) device regulated under 21 CFR 892.1000.