INOMAX DS (DELIVERY SYSTEM)
K-Number: K121021 · 2012-09-24
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Device Summary
Frequently Asked Questions
What is the INOMAX DS (DELIVERY SYSTEM)?
INOMAX DS (DELIVERY SYSTEM) is a medical device that received FDA 510(k) clearance on 2012-09-24. The listed applicant is Ino Therapeutics. The 510(k) number is K121021.
When did INOMAX DS (DELIVERY SYSTEM) receive FDA 510(k) clearance?
INOMAX DS (DELIVERY SYSTEM) received FDA 510(k) clearance on 2012-09-24, under 510(k) number K121021.
Who is the listed applicant for INOMAX DS (DELIVERY SYSTEM)?
The FDA 510(k) record lists Ino Therapeutics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INOMAX DS (DELIVERY SYSTEM)?
The FDA product code for INOMAX DS (DELIVERY 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 Ino Therapeutics 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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