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FDA 510(k)

PM-80 PULMOTESTER

K-Number: K843984 · 1984-10-24

ApplicantFuture Impex Corp.
Decision Date1984-10-24
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PM-80 PULMOTESTER is the device name listed in this FDA 510(k) record. The listed applicant is Future Impex Corp.. It received FDA 510(k) clearance on 1984-10-24 under 510(k) number K843984. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PM-80 PULMOTESTER?

PM-80 PULMOTESTER is a medical device that received FDA 510(k) clearance on 1984-10-24. The listed applicant is Future Impex Corp.. The 510(k) number is K843984.

When did PM-80 PULMOTESTER receive FDA 510(k) clearance?

PM-80 PULMOTESTER received FDA 510(k) clearance on 1984-10-24, under 510(k) number K843984.

Who is the listed applicant for PM-80 PULMOTESTER?

The FDA 510(k) record lists Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PM-80 PULMOTESTER?

The FDA product code for PM-80 PULMOTESTER is BZG.

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Other records listing Future Impex Corp. 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.

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Related Devices (Code: BZG)

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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