TYPE YC ENDOCARDIAL LEAD
K-Number: K810491 · 1981-03-20
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Device Summary
Frequently Asked Questions
What is the TYPE YC ENDOCARDIAL LEAD?
TYPE YC ENDOCARDIAL LEAD is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Biotronik Sales, Inc.. The 510(k) number is K810491.
When did TYPE YC ENDOCARDIAL LEAD receive FDA 510(k) clearance?
TYPE YC ENDOCARDIAL LEAD received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810491.
Who is the listed applicant for TYPE YC ENDOCARDIAL LEAD?
The FDA 510(k) record lists Biotronik Sales, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TYPE YC ENDOCARDIAL LEAD?
The FDA product code for TYPE YC ENDOCARDIAL LEAD is DTB.
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 Biotronik Sales, 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: DTB)
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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