MASIMO SET USPO2 PULSE OXIMETRY CABLE
K-Number: K121914 · 2012-09-07
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Device Summary
Frequently Asked Questions
What is the MASIMO SET USPO2 PULSE OXIMETRY CABLE?
MASIMO SET USPO2 PULSE OXIMETRY CABLE is a medical device that received FDA 510(k) clearance on 2012-09-07. The listed applicant is Masimo Corporation. The 510(k) number is K121914.
When did MASIMO SET USPO2 PULSE OXIMETRY CABLE receive FDA 510(k) clearance?
MASIMO SET USPO2 PULSE OXIMETRY CABLE received FDA 510(k) clearance on 2012-09-07, under 510(k) number K121914.
Who is the listed applicant for MASIMO SET USPO2 PULSE OXIMETRY CABLE?
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 USPO2 PULSE OXIMETRY CABLE?
The FDA product code for MASIMO SET USPO2 PULSE OXIMETRY CABLE 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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