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FDA 510(k)

ATLANTIS GUI

K-Number: K924575 · 1993-03-04

ApplicantHospitronics
Decision Date1993-03-04
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ATLANTIS GUI is the device name listed in this FDA 510(k) record. The listed applicant is Hospitronics. It received FDA 510(k) clearance on 1993-03-04 under 510(k) number K924575. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATLANTIS GUI?

ATLANTIS GUI is a medical device that received FDA 510(k) clearance on 1993-03-04. The listed applicant is Hospitronics. The 510(k) number is K924575.

When did ATLANTIS GUI receive FDA 510(k) clearance?

ATLANTIS GUI received FDA 510(k) clearance on 1993-03-04, under 510(k) number K924575.

Who is the listed applicant for ATLANTIS GUI?

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

What is the FDA product code for ATLANTIS GUI?

The FDA product code for ATLANTIS GUI is MHX.

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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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