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FDA 510(k)

MT/S (SOFTWARE RELEASE 3.1)

K-Number: K884607 · 1988-12-21

ApplicantDiasonics, Inc.
Decision Date1988-12-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MT/S (SOFTWARE RELEASE 3.1) is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1988-12-21 under 510(k) number K884607. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MT/S (SOFTWARE RELEASE 3.1)?

MT/S (SOFTWARE RELEASE 3.1) is a medical device that received FDA 510(k) clearance on 1988-12-21. The listed applicant is Diasonics, Inc.. The 510(k) number is K884607.

When did MT/S (SOFTWARE RELEASE 3.1) receive FDA 510(k) clearance?

MT/S (SOFTWARE RELEASE 3.1) received FDA 510(k) clearance on 1988-12-21, under 510(k) number K884607.

Who is the listed applicant for MT/S (SOFTWARE RELEASE 3.1)?

The FDA 510(k) record lists Diasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MT/S (SOFTWARE RELEASE 3.1)?

The FDA product code for MT/S (SOFTWARE RELEASE 3.1) is LNH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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