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FDA 510(k)

NASAL OXYGEN CANNULA, #017207

K-Number: K771074 · 1977-08-04

Decision Date1977-08-04
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NASAL OXYGEN CANNULA, #017207 is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771074. 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 NASAL OXYGEN CANNULA, #017207?

NASAL OXYGEN CANNULA, #017207 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K771074.

When did NASAL OXYGEN CANNULA, #017207 receive FDA 510(k) clearance?

NASAL OXYGEN CANNULA, #017207 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771074.

Who is the listed applicant for NASAL OXYGEN CANNULA, #017207?

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

What is the FDA product code for NASAL OXYGEN CANNULA, #017207?

The FDA product code for NASAL OXYGEN CANNULA, #017207 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 C.R. Bard, 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: 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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