URI-CATH SYSTEM
K-Number: K852490 · 1985-11-05
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Device Summary
Frequently Asked Questions
What is the URI-CATH SYSTEM?
URI-CATH SYSTEM is a medical device that received FDA 510(k) clearance on 1985-11-05. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K852490.
When did URI-CATH SYSTEM receive FDA 510(k) clearance?
URI-CATH SYSTEM received FDA 510(k) clearance on 1985-11-05, under 510(k) number K852490.
Who is the listed applicant for URI-CATH SYSTEM?
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 URI-CATH SYSTEM?
The FDA product code for URI-CATH SYSTEM is KNX.
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: KNX)
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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