CATH CADDIE
K-Number: K961884 · 1996-08-01
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Device Summary
Frequently Asked Questions
What is the CATH CADDIE?
CATH CADDIE is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Mark-Clark. The 510(k) number is K961884.
When did CATH CADDIE receive FDA 510(k) clearance?
CATH CADDIE received FDA 510(k) clearance on 1996-08-01, under 510(k) number K961884.
Who is the listed applicant for CATH CADDIE?
The FDA 510(k) record lists Mark-Clark as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATH CADDIE?
The FDA product code for CATH CADDIE is KNT.
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 Mark-Clark 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: KNT)
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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