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FDA 510(k)

HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER

K-Number: K110752 · 2011-06-28

ApplicantHighland Instruments
Decision Date2011-06-28
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Highland Instruments. It received FDA 510(k) clearance on 2011-06-28 under 510(k) number K110752. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER?

HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER is a medical device that received FDA 510(k) clearance on 2011-06-28. The listed applicant is Highland Instruments. The 510(k) number is K110752.

When did HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER receive FDA 510(k) clearance?

HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER received FDA 510(k) clearance on 2011-06-28, under 510(k) number K110752.

Who is the listed applicant for HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER?

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

What is the FDA product code for HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER?

The FDA product code for HIGHLAND INSTRUMENTS CES AND TUS INSTRUMENT HOLDER is ITX.

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Related Devices (Code: ITX)

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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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