FDA 510(k)

Endiscope, Endiscope Cervical

K-Number: K180766 · 2018-06-11

Decision Date2018-06-11

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Endiscope, Endiscope Cervical is a medical device manufactured by Elliquence, LLC. It received FDA 510(k) clearance on 2018-06-11 under approval number K180766. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endiscope, Endiscope Cervical?

Endiscope, Endiscope Cervical is a medical device that received FDA 510(k) clearance on 2018-06-11. It is manufactured by Elliquence, LLC. The 510(k) number is K180766.

When was Endiscope, Endiscope Cervical approved by the FDA?

Endiscope, Endiscope Cervical received FDA 510(k) clearance on 2018-06-11, under approval number K180766.

What company makes Endiscope, Endiscope Cervical?

Endiscope, Endiscope Cervical is manufactured by Elliquence, LLC.

What is the FDA product code for Endiscope, Endiscope Cervical?

The FDA product code for Endiscope, Endiscope Cervical is HRX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.