CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020
K-Number: K041574 · 2004-07-12
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Device Summary
Frequently Asked Questions
What is the CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020?
CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020 is a medical device that received FDA 510(k) clearance on 2004-07-12. The listed applicant is Guidant Corporation. The 510(k) number is K041574.
When did CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020 receive FDA 510(k) clearance?
CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020 received FDA 510(k) clearance on 2004-07-12, under 510(k) number K041574.
Who is the listed applicant for CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020?
The FDA 510(k) record lists Guidant Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020?
The FDA product code for CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020 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 Guidant Corporation 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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