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FDA 510(k)

INTEGRATED PATIENT MONITORING SYSTEM

K-Number: K041918 · 2004-10-15

ApplicantInvivo Research, Inc.
Decision Date2004-10-15
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTEGRATED PATIENT MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Research, Inc.. It received FDA 510(k) clearance on 2004-10-15 under 510(k) number K041918. 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 INTEGRATED PATIENT MONITORING SYSTEM?

INTEGRATED PATIENT MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-15. The listed applicant is Invivo Research, Inc.. The 510(k) number is K041918.

When did INTEGRATED PATIENT MONITORING SYSTEM receive FDA 510(k) clearance?

INTEGRATED PATIENT MONITORING SYSTEM received FDA 510(k) clearance on 2004-10-15, under 510(k) number K041918.

Who is the listed applicant for INTEGRATED PATIENT MONITORING SYSTEM?

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

What is the FDA product code for INTEGRATED PATIENT MONITORING SYSTEM?

The FDA product code for INTEGRATED PATIENT MONITORING SYSTEM is MWI.

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Other records listing Invivo Research, Inc. as applicant

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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

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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