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FDA 510(k)

PULMONARY TEST SYSTEM FUDAC-30

K-Number: K852307 · 1985-07-05

ApplicantFuturemed Div. of Future Impex Corp.
Decision Date1985-07-05
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PULMONARY TEST SYSTEM FUDAC-30 is the device name listed in this FDA 510(k) record. The listed applicant is Futuremed Div. of Future Impex Corp.. It received FDA 510(k) clearance on 1985-07-05 under 510(k) number K852307. 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 PULMONARY TEST SYSTEM FUDAC-30?

PULMONARY TEST SYSTEM FUDAC-30 is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K852307.

When did PULMONARY TEST SYSTEM FUDAC-30 receive FDA 510(k) clearance?

PULMONARY TEST SYSTEM FUDAC-30 received FDA 510(k) clearance on 1985-07-05, under 510(k) number K852307.

Who is the listed applicant for PULMONARY TEST SYSTEM FUDAC-30?

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

What is the FDA product code for PULMONARY TEST SYSTEM FUDAC-30?

The FDA product code for PULMONARY TEST SYSTEM FUDAC-30 is BZG.

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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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