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FDA 510(k)

MODEL 640GE-64: QUADRATURE PELVIC COIL

K-Number: K930674 · 1993-09-16

ApplicantMedical Advances, Inc.
Decision Date1993-09-16
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 640GE-64: QUADRATURE PELVIC COIL 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 1993-09-16 under 510(k) number K930674. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 640GE-64: QUADRATURE PELVIC COIL?

MODEL 640GE-64: QUADRATURE PELVIC COIL is a medical device that received FDA 510(k) clearance on 1993-09-16. The listed applicant is Medical Advances, Inc.. The 510(k) number is K930674.

When did MODEL 640GE-64: QUADRATURE PELVIC COIL receive FDA 510(k) clearance?

MODEL 640GE-64: QUADRATURE PELVIC COIL received FDA 510(k) clearance on 1993-09-16, under 510(k) number K930674.

Who is the listed applicant for MODEL 640GE-64: QUADRATURE PELVIC COIL?

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 MODEL 640GE-64: QUADRATURE PELVIC COIL?

The FDA product code for MODEL 640GE-64: QUADRATURE PELVIC COIL is LNH.

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Other records listing Medical Advances, Inc. as applicant

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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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