CORDIPAK ANGIOGRAPHY TRAY
K-Number: K863336 · 1986-09-12
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Device Summary
Frequently Asked Questions
What is the CORDIPAK ANGIOGRAPHY TRAY?
CORDIPAK ANGIOGRAPHY TRAY is a medical device that received FDA 510(k) clearance on 1986-09-12. The listed applicant is Angi-Pak Corp.. The 510(k) number is K863336.
When did CORDIPAK ANGIOGRAPHY TRAY receive FDA 510(k) clearance?
CORDIPAK ANGIOGRAPHY TRAY received FDA 510(k) clearance on 1986-09-12, under 510(k) number K863336.
Who is the listed applicant for CORDIPAK ANGIOGRAPHY TRAY?
The FDA 510(k) record lists Angi-Pak Corp. as the applicant. This does not by itself establish the device manufacturer.
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 Angi-Pak 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.
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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