SENSORMEDICS OXYSHUTTLE II(TM)
K-Number: K913790 · 1992-02-26
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Device Summary
Frequently Asked Questions
What is the SENSORMEDICS OXYSHUTTLE II(TM)?
SENSORMEDICS OXYSHUTTLE II(TM) is a medical device that received FDA 510(k) clearance on 1992-02-26. The listed applicant is Sensor Medics Corp.. The 510(k) number is K913790.
When did SENSORMEDICS OXYSHUTTLE II(TM) receive FDA 510(k) clearance?
SENSORMEDICS OXYSHUTTLE II(TM) received FDA 510(k) clearance on 1992-02-26, under 510(k) number K913790.
Who is the listed applicant for SENSORMEDICS OXYSHUTTLE II(TM)?
The FDA 510(k) record lists Sensor Medics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENSORMEDICS OXYSHUTTLE II(TM)?
The FDA product code for SENSORMEDICS OXYSHUTTLE II(TM) 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 Sensor Medics Corp. 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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