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FDA 510(k)

MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES

K-Number: K091057 · 2009-07-09

ApplicantMasimo Corporation
Decision Date2009-07-09
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Masimo Corporation. It received FDA 510(k) clearance on 2009-07-09 under 510(k) number K091057. 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 RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES?

MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2009-07-09. The listed applicant is Masimo Corporation. The 510(k) number is K091057.

When did MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES receive FDA 510(k) clearance?

MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES received FDA 510(k) clearance on 2009-07-09, under 510(k) number K091057.

Who is the listed applicant for MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES?

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 RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES?

The FDA product code for MASIMO RAINBOW SET PRONTO PULSE CO-OXIMETER AND ACCESSORIES is DQA.

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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.

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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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