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FDA 510(k)

AEROSOL & OXYGEN MASKS

K-Number: K772141 · 1978-01-03

Decision Date1978-01-03
Product CodeBYG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AEROSOL & OXYGEN MASKS 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 1978-01-03 under 510(k) number K772141. The device is classified under product code BYG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROSOL & OXYGEN MASKS?

AEROSOL & OXYGEN MASKS is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K772141.

When did AEROSOL & OXYGEN MASKS receive FDA 510(k) clearance?

AEROSOL & OXYGEN MASKS received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772141.

Who is the listed applicant for AEROSOL & OXYGEN MASKS?

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 AEROSOL & OXYGEN MASKS?

The FDA product code for AEROSOL & OXYGEN MASKS is BYG.

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: BYG)

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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