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)

VENTILATOR TEST LUNG

K-Number: K800125 · 1980-01-24

Decision Date1980-01-24
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILATOR TEST LUNG is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Med Devices, Inc.. It received FDA 510(k) clearance on 1980-01-24 under 510(k) number K800125. 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 VENTILATOR TEST LUNG?

VENTILATOR TEST LUNG is a medical device that received FDA 510(k) clearance on 1980-01-24. The listed applicant is Bio-Med Devices, Inc.. The 510(k) number is K800125.

When did VENTILATOR TEST LUNG receive FDA 510(k) clearance?

VENTILATOR TEST LUNG received FDA 510(k) clearance on 1980-01-24, under 510(k) number K800125.

Who is the listed applicant for VENTILATOR TEST LUNG?

The FDA 510(k) record lists Bio-Med Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTILATOR TEST LUNG?

The FDA product code for VENTILATOR TEST LUNG 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 Bio-Med Devices, 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 14 devices →

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.

↑