MASIMO SET RADICAL 7 PULSE CO-OXIMETER
K-Number: K061204 · 2006-07-27
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Device Summary
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.
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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