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FDA 510(k)

UPGRADED SPIROMETER ST-90

K-Number: K933511 · 1994-02-10

ApplicantFuturemed Div. of Future Impex Corp.
Decision Date1994-02-10
Product CodeBTY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UPGRADED SPIROMETER ST-90 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 1994-02-10 under 510(k) number K933511. The device is classified under product code BTY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UPGRADED SPIROMETER ST-90?

UPGRADED SPIROMETER ST-90 is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K933511.

When did UPGRADED SPIROMETER ST-90 receive FDA 510(k) clearance?

UPGRADED SPIROMETER ST-90 received FDA 510(k) clearance on 1994-02-10, under 510(k) number K933511.

Who is the listed applicant for UPGRADED SPIROMETER ST-90?

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 UPGRADED SPIROMETER ST-90?

The FDA product code for UPGRADED SPIROMETER ST-90 is BTY.

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Other records listing Futuremed Div. of Future Impex Corp. as applicant

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Related Devices (Code: BTY)

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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