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FDA 510(k)

PHASED ARRAY FLEXIBLE CARDIAC COIL

K-Number: K984588 · 1999-02-08

Decision Date1999-02-08
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHASED ARRAY FLEXIBLE CARDIAC COIL is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1999-02-08 under 510(k) number K984588. 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 PHASED ARRAY FLEXIBLE CARDIAC COIL?

PHASED ARRAY FLEXIBLE CARDIAC COIL is a medical device that received FDA 510(k) clearance on 1999-02-08. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K984588.

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

PHASED ARRAY FLEXIBLE CARDIAC COIL received FDA 510(k) clearance on 1999-02-08, under 510(k) number K984588.

Who is the listed applicant for PHASED ARRAY FLEXIBLE CARDIAC COIL?

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

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

The FDA product code for PHASED ARRAY FLEXIBLE CARDIAC 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 Philips Medical Systems (Cleveland), 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.

View all 190 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

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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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