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FDA 510(k)

INOMAX DS (DELIVERY SYSTEM), MODEL 10003

K-Number: K080484 · 2008-08-06

ApplicantIno Therapeutics
Decision Date2008-08-06
Product CodeMRN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INOMAX DS (DELIVERY SYSTEM), MODEL 10003 is the device name listed in this FDA 510(k) record. The listed applicant is Ino Therapeutics. It received FDA 510(k) clearance on 2008-08-06 under 510(k) number K080484. The device is classified under product code MRN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INOMAX DS (DELIVERY SYSTEM), MODEL 10003?

INOMAX DS (DELIVERY SYSTEM), MODEL 10003 is a medical device that received FDA 510(k) clearance on 2008-08-06. The listed applicant is Ino Therapeutics. The 510(k) number is K080484.

When did INOMAX DS (DELIVERY SYSTEM), MODEL 10003 receive FDA 510(k) clearance?

INOMAX DS (DELIVERY SYSTEM), MODEL 10003 received FDA 510(k) clearance on 2008-08-06, under 510(k) number K080484.

Who is the listed applicant for INOMAX DS (DELIVERY SYSTEM), MODEL 10003?

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), MODEL 10003?

The FDA product code for INOMAX DS (DELIVERY SYSTEM), MODEL 10003 is MRN.

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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.

K130605INOMAX DSIR (DELIVERY SYSTEM)K122689INOBLENDERK121021INOMAX DS (DELIVERY SYSTEM)K110344INOMAX DSIR (DELIVERY SYSTEM)K093922INOMAX DSK061901INO THERAPEUTICS INOMAX DS (DELIVERY SYSTEM), MODEL 10003

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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.

K242374ULSPIRA TS™ Nitric Oxide Therapy SystemAirgas Therapeutics, LLCK242578EVOLVE Nitric Oxide Delivery SystemMallinckrodt Manufacturing, LLCK240410EVOLVE Nitric Oxide Delivery SystemMalinckrodt Manufacturing, LLCK233251NOxBOXi Nitric Oxide Delivery SystemLinde Gas & Equipment, Inc.K222930Evolve Nitric Oxide Delivery SystemMallinckrodt Manufacturing, LLCK231823NOxBOXi Nitric Oxide Delivery SystemLinde Gas & Equipment, Inc.

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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