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FDA 510(k)

CANNULA, ARGYLE NASAL OXYGEN

K-Number: K760337 · 1976-08-11

Decision Date1976-08-11
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CANNULA, ARGYLE NASAL OXYGEN is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760337. 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 CANNULA, ARGYLE NASAL OXYGEN?

CANNULA, ARGYLE NASAL OXYGEN is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760337.

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

CANNULA, ARGYLE NASAL OXYGEN received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760337.

Who is the listed applicant for CANNULA, ARGYLE NASAL OXYGEN?

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

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

The FDA product code for CANNULA, ARGYLE NASAL OXYGEN 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 Sherwood Medical Industries 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.

View all 62 devices →

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

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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