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FDA 510(k)

CANNULA NASAL OXYGEN

K-Number: K920573 · 1992-08-11

Decision Date1992-08-11
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CANNULA NASAL OXYGEN is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1992-08-11 under 510(k) number K920573. 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 NASAL OXYGEN?

CANNULA NASAL OXYGEN is a medical device that received FDA 510(k) clearance on 1992-08-11. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K920573.

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

CANNULA NASAL OXYGEN received FDA 510(k) clearance on 1992-08-11, under 510(k) number K920573.

Who is the listed applicant for CANNULA NASAL OXYGEN?

The FDA 510(k) record lists B & F Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANNULA NASAL OXYGEN?

The FDA product code for CANNULA 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 B & F Medical Products, 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.

View all 18 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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