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FDA 510(k)

CAC-127-8 CARDOAC ARRAY COIL

K-Number: K051512 · 2005-06-28

ApplicantInvivo Corp.
Decision Date2005-06-28
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAC-127-8 CARDOAC ARRAY COIL is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corp.. It received FDA 510(k) clearance on 2005-06-28 under 510(k) number K051512. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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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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