ADAPTER, CORDIS
K-Number: K770478 · 1977-03-30
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Device Summary
Frequently Asked Questions
What is the ADAPTER, CORDIS?
ADAPTER, CORDIS is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Cordis Corp.. The 510(k) number is K770478.
When did ADAPTER, CORDIS receive FDA 510(k) clearance?
ADAPTER, CORDIS received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770478.
Who is the listed applicant for ADAPTER, CORDIS?
The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADAPTER, CORDIS?
The FDA product code for ADAPTER, CORDIS is DTD.
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 Cordis 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: DTD)
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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