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FDA 510(k)

FUKUNDA SANGYO UNITS ELECTRONIC SPIRO

K-Number: K832430 · 1983-09-29

ApplicantFuture Impex Corp.
Decision Date1983-09-29
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FUKUNDA SANGYO UNITS ELECTRONIC SPIRO 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 1983-09-29 under 510(k) number K832430. 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 FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

FUKUNDA SANGYO UNITS ELECTRONIC SPIRO is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Future Impex Corp.. The 510(k) number is K832430.

When did FUKUNDA SANGYO UNITS ELECTRONIC SPIRO receive FDA 510(k) clearance?

FUKUNDA SANGYO UNITS ELECTRONIC SPIRO received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832430.

Who is the listed applicant for FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

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 FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

The FDA product code for FUKUNDA SANGYO UNITS ELECTRONIC SPIRO 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.

K861487ST-90 SPIRO ANALIZERK854687ERMA HB-METER MODEL 303NK854686TE-25 COAGURO METERK854685DIGITAL-9 KEY LEUCOCYTE COUNTERK854677ERMA PC-604 BLOOD CELL COUNTERK854678ERMA PC-602 PC-603 BLOOD CELL COUNTER

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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.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

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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