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FDA 510(k)

TEMPOROMANIBULAR COIL 15

K-Number: K110373 · 2011-04-06

ApplicantEsaote, S.p.A.
Decision Date2011-04-06
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TEMPOROMANIBULAR COIL 15 is the device name listed in this FDA 510(k) record. The listed applicant is Esaote, S.p.A.. It received FDA 510(k) clearance on 2011-04-06 under 510(k) number K110373. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPOROMANIBULAR COIL 15?

TEMPOROMANIBULAR COIL 15 is a medical device that received FDA 510(k) clearance on 2011-04-06. The listed applicant is Esaote, S.p.A.. The 510(k) number is K110373.

When did TEMPOROMANIBULAR COIL 15 receive FDA 510(k) clearance?

TEMPOROMANIBULAR COIL 15 received FDA 510(k) clearance on 2011-04-06, under 510(k) number K110373.

Who is the listed applicant for TEMPOROMANIBULAR COIL 15?

The FDA 510(k) record lists Esaote, S.p.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMPOROMANIBULAR COIL 15?

The FDA product code for TEMPOROMANIBULAR COIL 15 is MOS.

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Related Devices (Code: MOS)

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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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