CAC-127-8 CARDOAC ARRAY COIL
K-Number: K051512 · 2005-06-28
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Device Summary
Frequently Asked Questions
What is the CAC-127-8 CARDOAC ARRAY COIL?
CAC-127-8 CARDOAC ARRAY COIL is a medical device that received FDA 510(k) clearance on 2005-06-28. The listed applicant is Invivo Corp.. The 510(k) number is K051512.
When did CAC-127-8 CARDOAC ARRAY COIL receive FDA 510(k) clearance?
CAC-127-8 CARDOAC ARRAY COIL received FDA 510(k) clearance on 2005-06-28, under 510(k) number K051512.
Who is the listed applicant for CAC-127-8 CARDOAC ARRAY COIL?
The FDA 510(k) record lists Invivo Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAC-127-8 CARDOAC ARRAY COIL?
The FDA product code for CAC-127-8 CARDOAC ARRAY COIL is MOS.
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 Invivo 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: MOS)
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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