CATHETER INTRODUCER
K-Number: K871153 · 1987-06-24
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Device Summary
Frequently Asked Questions
What is the CATHETER INTRODUCER?
CATHETER INTRODUCER is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Angeion Corp.. The 510(k) number is K871153.
When did CATHETER INTRODUCER receive FDA 510(k) clearance?
CATHETER INTRODUCER received FDA 510(k) clearance on 1987-06-24, under 510(k) number K871153.
Who is the listed applicant for CATHETER INTRODUCER?
The FDA 510(k) record lists Angeion Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETER INTRODUCER?
The FDA product code for CATHETER INTRODUCER is DYB.
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 Angeion 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: DYB)
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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