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FDA 510(k)

MASIMO PATIENT SAFETY NET

K-Number: K071047 · 2007-06-08

Decision Date2007-06-08
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MASIMO PATIENT SAFETY NET is the device name listed in this FDA 510(k) record. The listed applicant is Masimo Corporation. It received FDA 510(k) clearance on 2007-06-08 under 510(k) number K071047. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASIMO PATIENT SAFETY NET?

MASIMO PATIENT SAFETY NET is a medical device that received FDA 510(k) clearance on 2007-06-08. The listed applicant is Masimo Corporation. The 510(k) number is K071047.

When did MASIMO PATIENT SAFETY NET receive FDA 510(k) clearance?

MASIMO PATIENT SAFETY NET received FDA 510(k) clearance on 2007-06-08, under 510(k) number K071047.

Who is the listed applicant for MASIMO PATIENT SAFETY NET?

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

What is the FDA product code for MASIMO PATIENT SAFETY NET?

The FDA product code for MASIMO PATIENT SAFETY NET is MSX.

Related Clinical Trials

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.

Other records listing Masimo Corporation 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 82 devices →

Related Devices (Code: MSX)

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

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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