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FDA 510(k)

LUNG POWER

K-Number: K832195 · 1983-10-18

ApplicantConsolidated Medical Technologies
Decision Date1983-10-18
Product Code
DecisionSubstantially Equivalent

Device Summary

LUNG POWER is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Medical Technologies. It received FDA 510(k) clearance on 1983-10-18 under 510(k) number K832195. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNG POWER?

LUNG POWER is a medical device that received FDA 510(k) clearance on 1983-10-18. The listed applicant is Consolidated Medical Technologies. The 510(k) number is K832195.

When did LUNG POWER receive FDA 510(k) clearance?

LUNG POWER received FDA 510(k) clearance on 1983-10-18, under 510(k) number K832195.

Who is the listed applicant for LUNG POWER?

The FDA 510(k) record lists Consolidated Medical Technologies as the applicant. This does not by itself establish the device manufacturer.

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.

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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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