AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM
K-Number: K093260 · 2009-12-16
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Device Summary
Frequently Asked Questions
What is the AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM?
AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2009-12-16. The listed applicant is International Biomedical, Ltd.. The 510(k) number is K093260.
When did AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM receive FDA 510(k) clearance?
AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM received FDA 510(k) clearance on 2009-12-16, under 510(k) number K093260.
Who is the listed applicant for AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM?
The FDA 510(k) record lists International Biomedical, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM?
The FDA product code for AERONOX NITRIC OXIDE TITRATION & MONITORING SYSTEM is MRN.
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 International Biomedical, Ltd. 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: MRN)
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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