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FDA 510(k)

MASIMO SET RADICAL 7 PULSE CO-OXIMETER

K-Number: K061204 · 2006-07-27

Decision Date2006-07-27
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MASIMO SET RADICAL 7 PULSE CO-OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Masimo Corporation. It received FDA 510(k) clearance on 2006-07-27 under 510(k) number K061204. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASIMO SET RADICAL 7 PULSE CO-OXIMETER?

MASIMO SET RADICAL 7 PULSE CO-OXIMETER is a medical device that received FDA 510(k) clearance on 2006-07-27. The listed applicant is Masimo Corporation. The 510(k) number is K061204.

When did MASIMO SET RADICAL 7 PULSE CO-OXIMETER receive FDA 510(k) clearance?

MASIMO SET RADICAL 7 PULSE CO-OXIMETER received FDA 510(k) clearance on 2006-07-27, under 510(k) number K061204.

Who is the listed applicant for MASIMO SET RADICAL 7 PULSE CO-OXIMETER?

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 SET RADICAL 7 PULSE CO-OXIMETER?

The FDA product code for MASIMO SET RADICAL 7 PULSE CO-OXIMETER is DQA.

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: DQA)

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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