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FDA 510(k)

CORDIPAK ANGIOGRAPHY TRAY

K-Number: K863336 · 1986-09-12

Decision Date1986-09-12
Product Code
DecisionSubstantially Equivalent

Device Summary

CORDIPAK ANGIOGRAPHY TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Angi-Pak Corp.. It received FDA 510(k) clearance on 1986-09-12 under 510(k) number K863336. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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