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FDA 510(k)

SPIRO ANALYZER ST-100 AUTOMATIC SPIRO

K-Number: K832432 · 1983-09-29

Decision Date1983-09-29
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPIRO ANALYZER ST-100 AUTOMATIC 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 K832432. 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 SPIRO ANALYZER ST-100 AUTOMATIC SPIRO?

SPIRO ANALYZER ST-100 AUTOMATIC 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 K832432.

When did SPIRO ANALYZER ST-100 AUTOMATIC SPIRO receive FDA 510(k) clearance?

SPIRO ANALYZER ST-100 AUTOMATIC SPIRO received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832432.

Who is the listed applicant for SPIRO ANALYZER ST-100 AUTOMATIC 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 SPIRO ANALYZER ST-100 AUTOMATIC SPIRO?

The FDA product code for SPIRO ANALYZER ST-100 AUTOMATIC SPIRO is BZG.

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.

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.

View all 14 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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