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FDA 510(k)

MODEL 6000-21; VOLUME NECK COIL

K-Number: K901384 · 1990-04-26

ApplicantMedical Advances, Inc.
Decision Date1990-04-26
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 6000-21; VOLUME NECK 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 1990-04-26 under 510(k) number K901384. 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 6000-21; VOLUME NECK COIL?

MODEL 6000-21; VOLUME NECK COIL is a medical device that received FDA 510(k) clearance on 1990-04-26. The listed applicant is Medical Advances, Inc.. The 510(k) number is K901384.

When did MODEL 6000-21; VOLUME NECK COIL receive FDA 510(k) clearance?

MODEL 6000-21; VOLUME NECK COIL received FDA 510(k) clearance on 1990-04-26, under 510(k) number K901384.

Who is the listed applicant for MODEL 6000-21; VOLUME NECK 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 6000-21; VOLUME NECK COIL?

The FDA product code for MODEL 6000-21; VOLUME NECK COIL is LNH.

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Other records listing Medical Advances, Inc. as applicant

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K023084MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COILK021433MODEL 415PH-64/42: PHASED ARRAY SHOULDER COILK011608MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COILK010074MODEL 455GE PHASED ARRAY WRIST COILK003685MODEL 342GE-64 HIGH RESOLUTION BRAIN COILK003144MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COIL

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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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