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FDA 510(k)

PATIENT MONITORS VARIOUS MODELS

K-Number: K151812 · 2016-01-26

Decision Date2016-01-26
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITORS VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2016-01-26 under 510(k) number K151812. 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 PATIENT MONITORS VARIOUS MODELS?

PATIENT MONITORS VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 2016-01-26. The listed applicant is Philips Medical Systems. The 510(k) number is K151812.

When did PATIENT MONITORS VARIOUS MODELS receive FDA 510(k) clearance?

PATIENT MONITORS VARIOUS MODELS received FDA 510(k) clearance on 2016-01-26, under 510(k) number K151812.

Who is the listed applicant for PATIENT MONITORS VARIOUS MODELS?

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

What is the FDA product code for PATIENT MONITORS VARIOUS MODELS?

The FDA product code for PATIENT MONITORS VARIOUS MODELS is MHX.

Other records listing Philips Medical Systems as applicant

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.

View all 17 devices →

Related Devices (Code: MHX)

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.

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.