PERCUTANEOUS INTRODUCER COURNAND STYLE
K-Number: K812973 · 1981-11-16
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Device Summary
Frequently Asked Questions
What is the PERCUTANEOUS INTRODUCER COURNAND STYLE?
PERCUTANEOUS INTRODUCER COURNAND STYLE is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Dip, Inc.. The 510(k) number is K812973.
When did PERCUTANEOUS INTRODUCER COURNAND STYLE receive FDA 510(k) clearance?
PERCUTANEOUS INTRODUCER COURNAND STYLE received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812973.
Who is the listed applicant for PERCUTANEOUS INTRODUCER COURNAND STYLE?
The FDA 510(k) record lists Dip, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERCUTANEOUS INTRODUCER COURNAND STYLE?
The FDA product code for PERCUTANEOUS INTRODUCER COURNAND STYLE 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 Dip, 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: 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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