GESCO ASPIRATOR
K-Number: K870962 · 1987-05-22
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Device Summary
Frequently Asked Questions
What is the GESCO ASPIRATOR?
GESCO ASPIRATOR is a medical device that received FDA 510(k) clearance on 1987-05-22. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K870962.
When did GESCO ASPIRATOR receive FDA 510(k) clearance?
GESCO ASPIRATOR received FDA 510(k) clearance on 1987-05-22, under 510(k) number K870962.
Who is the listed applicant for GESCO ASPIRATOR?
The FDA 510(k) record lists Gesco Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GESCO ASPIRATOR?
The FDA product code for GESCO ASPIRATOR is BSY.
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 Gesco Intl., Inc. 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: BSY)
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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