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FDA 510(k)

8 CHANNEL CARDIAC PHASED ARRAY COIL

K-Number: K032045 · 2003-07-30

Decision Date2003-07-30
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

8 CHANNEL CARDIAC PHASED ARRAY COIL is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 2003-07-30 under 510(k) number K032045. 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 8 CHANNEL CARDIAC PHASED ARRAY COIL?

8 CHANNEL CARDIAC PHASED ARRAY COIL is a medical device that received FDA 510(k) clearance on 2003-07-30. The listed applicant is GE Medical Systems. The 510(k) number is K032045.

When did 8 CHANNEL CARDIAC PHASED ARRAY COIL receive FDA 510(k) clearance?

8 CHANNEL CARDIAC PHASED ARRAY COIL received FDA 510(k) clearance on 2003-07-30, under 510(k) number K032045.

Who is the listed applicant for 8 CHANNEL CARDIAC PHASED ARRAY COIL?

The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 8 CHANNEL CARDIAC PHASED ARRAY COIL?

The FDA product code for 8 CHANNEL CARDIAC PHASED 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 GE Medical Systems 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.

View all 170 devices →

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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