CLOSED FOLEY CATHETER SYSTEM
K-Number: K873288 · 1987-11-27
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Device Summary
Frequently Asked Questions
What is the CLOSED FOLEY CATHETER SYSTEM?
CLOSED FOLEY CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 1987-11-27. The listed applicant is Todd Medical, Inc.. The 510(k) number is K873288.
When did CLOSED FOLEY CATHETER SYSTEM receive FDA 510(k) clearance?
CLOSED FOLEY CATHETER SYSTEM received FDA 510(k) clearance on 1987-11-27, under 510(k) number K873288.
Who is the listed applicant for CLOSED FOLEY CATHETER SYSTEM?
The FDA 510(k) record lists Todd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLOSED FOLEY CATHETER SYSTEM?
The FDA product code for CLOSED FOLEY CATHETER SYSTEM is KNY.
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 Todd Medical, 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: KNY)
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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