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FDA 510(k)

VERSION 4.2 APPLICATION SOFTWARE

K-Number: K892959 · 1989-06-01

ApplicantResonex, Inc.
Decision Date1989-06-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VERSION 4.2 APPLICATION SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1989-06-01 under 510(k) number K892959. 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 VERSION 4.2 APPLICATION SOFTWARE?

VERSION 4.2 APPLICATION SOFTWARE is a medical device that received FDA 510(k) clearance on 1989-06-01. The listed applicant is Resonex, Inc.. The 510(k) number is K892959.

When did VERSION 4.2 APPLICATION SOFTWARE receive FDA 510(k) clearance?

VERSION 4.2 APPLICATION SOFTWARE received FDA 510(k) clearance on 1989-06-01, under 510(k) number K892959.

Who is the listed applicant for VERSION 4.2 APPLICATION SOFTWARE?

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

What is the FDA product code for VERSION 4.2 APPLICATION SOFTWARE?

The FDA product code for VERSION 4.2 APPLICATION SOFTWARE is LNH.

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Other records listing Resonex, Inc. as applicant

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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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