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FDA 510(k)

SENSOR GUI

K-Number: K923519 · 1992-12-08

ApplicantHospitronic
Decision Date1992-12-08
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSOR GUI is the device name listed in this FDA 510(k) record. The listed applicant is Hospitronic. It received FDA 510(k) clearance on 1992-12-08 under 510(k) number K923519. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOR GUI?

SENSOR GUI is a medical device that received FDA 510(k) clearance on 1992-12-08. The listed applicant is Hospitronic. The 510(k) number is K923519.

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

SENSOR GUI received FDA 510(k) clearance on 1992-12-08, under 510(k) number K923519.

Who is the listed applicant for SENSOR GUI?

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

What is the FDA product code for SENSOR GUI?

The FDA product code for SENSOR GUI is BSZ.

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Related Devices (Code: BSZ)

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Official Source

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

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