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FDA 510(k)

MASK ARTIFICIAL RESPIRATION

K-Number: K760941 · 1977-01-12

ApplicantGene R. Baldwin
Decision Date1977-01-12
Product CodeBYG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASK ARTIFICIAL RESPIRATION is the device name listed in this FDA 510(k) record. The listed applicant is Gene R. Baldwin. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K760941. 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 MASK ARTIFICIAL RESPIRATION?

MASK ARTIFICIAL RESPIRATION is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Gene R. Baldwin. The 510(k) number is K760941.

When did MASK ARTIFICIAL RESPIRATION receive FDA 510(k) clearance?

MASK ARTIFICIAL RESPIRATION received FDA 510(k) clearance on 1977-01-12, under 510(k) number K760941.

Who is the listed applicant for MASK ARTIFICIAL RESPIRATION?

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

What is the FDA product code for MASK ARTIFICIAL RESPIRATION?

The FDA product code for MASK ARTIFICIAL RESPIRATION is BYG.

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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.

K963298FIRST AID KIT(S)Vector, Inc.K962848HANS RUDOLPH NASAL CPAP MASKHans Rudolph, Inc.K945482DISPOSABLE, CPAP OXYGEN MASKFvtnksK953464WESTMED PEDIATRIC & ADULT MEDIUM CONCENTRATION OXYGEN MASKWestmed, Inc.K953039VARIOUS ADULT & CHILD HIGH CON/NONREBREATH OXY MASKSDadsun Corp., Ltd.K945472WESTMED PEDIATRIC AND ADULT AEROSOL MASKWestmed Intl.

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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