Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR

K-Number: K792564 · 1979-12-19

Decision Date1979-12-19
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Eastern Anesthesia, Inc.. It received FDA 510(k) clearance on 1979-12-19 under 510(k) number K792564. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR?

MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR is a medical device that received FDA 510(k) clearance on 1979-12-19. The listed applicant is Eastern Anesthesia, Inc.. The 510(k) number is K792564.

When did MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR receive FDA 510(k) clearance?

MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR received FDA 510(k) clearance on 1979-12-19, under 510(k) number K792564.

Who is the listed applicant for MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR?

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

What is the FDA product code for MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR?

The FDA product code for MA-1 VENTILATOR & TIMETER AIRCOMPRESSOR is CBK.

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 Eastern Anesthesia, 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.

Related Devices (Code: CBK)

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.

↑