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FDA 510(k)

INTEGRITI PATIENT MONITOR

K-Number: K980688 · 1999-03-16

ApplicantAlliance Instruments
Decision Date1999-03-16
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTEGRITI PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Instruments. It received FDA 510(k) clearance on 1999-03-16 under 510(k) number K980688. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRITI PATIENT MONITOR?

INTEGRITI PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1999-03-16. The listed applicant is Alliance Instruments. The 510(k) number is K980688.

When did INTEGRITI PATIENT MONITOR receive FDA 510(k) clearance?

INTEGRITI PATIENT MONITOR received FDA 510(k) clearance on 1999-03-16, under 510(k) number K980688.

Who is the listed applicant for INTEGRITI PATIENT MONITOR?

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

What is the FDA product code for INTEGRITI PATIENT MONITOR?

The FDA product code for INTEGRITI PATIENT MONITOR is MWI.

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Related Devices (Code: MWI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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