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FDA 510(k)

VFQ HEAD COIL

K-Number: K883737 · 1988-10-13

ApplicantResonex, Inc.
Decision Date1988-10-13
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VFQ HEAD COIL is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1988-10-13 under 510(k) number K883737. 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 VFQ HEAD COIL?

VFQ HEAD COIL is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is Resonex, Inc.. The 510(k) number is K883737.

When did VFQ HEAD COIL receive FDA 510(k) clearance?

VFQ HEAD COIL received FDA 510(k) clearance on 1988-10-13, under 510(k) number K883737.

Who is the listed applicant for VFQ HEAD COIL?

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

What is the FDA product code for VFQ HEAD COIL?

The FDA product code for VFQ HEAD COIL is LNH.

Other records listing Resonex, 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.

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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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