MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS
K-Number: K053477 · 2006-03-16
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Device Summary
Frequently Asked Questions
What is the MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS?
MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS is a medical device that received FDA 510(k) clearance on 2006-03-16. The listed applicant is Masimo Corporation. The 510(k) number is K053477.
When did MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS receive FDA 510(k) clearance?
MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS received FDA 510(k) clearance on 2006-03-16, under 510(k) number K053477.
Who is the listed applicant for MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS?
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 RAD 57 CM AND M PULSE CO-OXIMETERS?
The FDA product code for MASIMO SET RAD 57 CM AND M PULSE CO-OXIMETERS 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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