FDA 510(k)

QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64

K-Number: K991724 · 1999-08-02

Decision Date1999-08-02

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Advances, Inc.. It received FDA 510(k) clearance on 1999-08-02 under 510(k) number K991724. 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 QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64?

QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64 is a medical device that received FDA 510(k) clearance on 1999-08-02. The listed applicant is Medical Advances, Inc.. The 510(k) number is K991724.

When did QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64 receive FDA 510(k) clearance?

QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64 received FDA 510(k) clearance on 1999-08-02, under 510(k) number K991724.

Who is the listed applicant for QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64?

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

What is the FDA product code for QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64?

The FDA product code for QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64 is MOS.

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Other records listing Medical Advances, Inc. as applicant

K023084MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL K021433MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL K011608MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COIL K010074MODEL 455GE PHASED ARRAY WRIST COIL K003685MODEL 342GE-64 HIGH RESOLUTION BRAIN COIL K003144MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COIL

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Related Devices (Code: MOS)

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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.