SPIRO ANALYZER ST-100 AUTOMATIC SPIRO
K-Number: K832432 · 1983-09-29
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Device Summary
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.
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
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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