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FDA 510(k)

Advincula Delineator Uterine Manipulator

K-Number: K180429 · 2018-03-14

Decision Date2018-03-14
Product CodeHEW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Advincula Delineator Uterine Manipulator is a medical device manufactured by CooperSurgical, Inc.. It received FDA 510(k) clearance on 2018-03-14 under approval number K180429. The device is classified under product code HEW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Advincula Delineator Uterine Manipulator?

Advincula Delineator Uterine Manipulator is a medical device that received FDA 510(k) clearance on 2018-03-14. It is manufactured by CooperSurgical, Inc.. The 510(k) number is K180429.

When was Advincula Delineator Uterine Manipulator approved by the FDA?

Advincula Delineator Uterine Manipulator received FDA 510(k) clearance on 2018-03-14, under approval number K180429.

What company makes Advincula Delineator Uterine Manipulator?

Advincula Delineator Uterine Manipulator is manufactured by CooperSurgical, Inc..

What is the FDA product code for Advincula Delineator Uterine Manipulator?

The FDA product code for Advincula Delineator Uterine Manipulator is HEW.

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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.