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FDA 510(k)

MEDISTOR III LUNG ANALYZER

K-Number: K800547 · 1980-03-25

Decision Date1980-03-25
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDISTOR III LUNG ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Cybermedic, Inc.. It received FDA 510(k) clearance on 1980-03-25 under 510(k) number K800547. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISTOR III LUNG ANALYZER?

MEDISTOR III LUNG ANALYZER is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is Cybermedic, Inc.. The 510(k) number is K800547.

When did MEDISTOR III LUNG ANALYZER receive FDA 510(k) clearance?

MEDISTOR III LUNG ANALYZER received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800547.

Who is the listed applicant for MEDISTOR III LUNG ANALYZER?

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

What is the FDA product code for MEDISTOR III LUNG ANALYZER?

The FDA product code for MEDISTOR III LUNG ANALYZER is BZC.

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 Cybermedic, 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 11 devices →

Related Devices (Code: BZC)

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

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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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