SPIRO ANALYZER ST-300
K-Number: K873817 · 1987-12-02
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Device Summary
Frequently Asked Questions
What is the SPIRO ANALYZER ST-300?
SPIRO ANALYZER ST-300 is a medical device that received FDA 510(k) clearance on 1987-12-02. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K873817.
When did SPIRO ANALYZER ST-300 receive FDA 510(k) clearance?
SPIRO ANALYZER ST-300 received FDA 510(k) clearance on 1987-12-02, under 510(k) number K873817.
Who is the listed applicant for SPIRO ANALYZER ST-300?
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 SPIRO ANALYZER ST-300?
The FDA product code for SPIRO ANALYZER ST-300 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 Futuremed Div. of 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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