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FDA 510(k)

BILATERAL TMJ COIL

K-Number: K902630 · 1990-07-19

ApplicantResonex, Inc.
Decision Date1990-07-19
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BILATERAL TMJ 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 1990-07-19 under 510(k) number K902630. 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 BILATERAL TMJ COIL?

BILATERAL TMJ COIL is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Resonex, Inc.. The 510(k) number is K902630.

When did BILATERAL TMJ COIL receive FDA 510(k) clearance?

BILATERAL TMJ COIL received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902630.

Who is the listed applicant for BILATERAL TMJ 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 BILATERAL TMJ COIL?

The FDA product code for BILATERAL TMJ COIL 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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