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FDA 510(k)

OECO NASAL CANNULA

K-Number: K811789 · 1981-07-02

ApplicantOeco
Decision Date1981-07-02
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OECO NASAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Oeco. It received FDA 510(k) clearance on 1981-07-02 under 510(k) number K811789. The device is classified under product code CAT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OECO NASAL CANNULA?

OECO NASAL CANNULA is a medical device that received FDA 510(k) clearance on 1981-07-02. The listed applicant is Oeco. The 510(k) number is K811789.

When did OECO NASAL CANNULA receive FDA 510(k) clearance?

OECO NASAL CANNULA received FDA 510(k) clearance on 1981-07-02, under 510(k) number K811789.

Who is the listed applicant for OECO NASAL CANNULA?

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

What is the FDA product code for OECO NASAL CANNULA?

The FDA product code for OECO NASAL CANNULA is CAT.

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 Oeco 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: CAT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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