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FDA 510(k)

COIL FIELD EXTENDER

K-Number: K911800 · 1991-07-03

ApplicantResonex, Inc.
Decision Date1991-07-03
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COIL FIELD EXTENDER is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1991-07-03 under 510(k) number K911800. 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 COIL FIELD EXTENDER?

COIL FIELD EXTENDER is a medical device that received FDA 510(k) clearance on 1991-07-03. The listed applicant is Resonex, Inc.. The 510(k) number is K911800.

When did COIL FIELD EXTENDER receive FDA 510(k) clearance?

COIL FIELD EXTENDER received FDA 510(k) clearance on 1991-07-03, under 510(k) number K911800.

Who is the listed applicant for COIL FIELD EXTENDER?

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 COIL FIELD EXTENDER?

The FDA product code for COIL FIELD EXTENDER is LNH.

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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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