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FDA 510(k)

OXYMATIC-24

K-Number: K884562 · 1989-01-09

ApplicantChad Therapeutics, Inc.
Decision Date1989-01-09
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYMATIC-24 is the device name listed in this FDA 510(k) record. The listed applicant is Chad Therapeutics, Inc.. It received FDA 510(k) clearance on 1989-01-09 under 510(k) number K884562. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYMATIC-24?

OXYMATIC-24 is a medical device that received FDA 510(k) clearance on 1989-01-09. The listed applicant is Chad Therapeutics, Inc.. The 510(k) number is K884562.

When did OXYMATIC-24 receive FDA 510(k) clearance?

OXYMATIC-24 received FDA 510(k) clearance on 1989-01-09, under 510(k) number K884562.

Who is the listed applicant for OXYMATIC-24?

The FDA 510(k) record lists Chad Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYMATIC-24?

The FDA product code for OXYMATIC-24 is NFB.

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Other records listing Chad Therapeutics, Inc. 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.

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Related Devices (Code: NFB)

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K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK221014Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileEffortless Oxygen, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter LabsK131023THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMENMedical Products, LLC

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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