FDA 510(k)

Miret Grasper, Alligator, Miret Grasper, Maryland

K-Number: K160149 · 2016-08-30

Decision Date2016-08-30

Product CodeOCW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Miret Grasper, Alligator, Miret Grasper, Maryland is a medical device manufactured by Miret Surgical, Inc.. It received FDA 510(k) clearance on 2016-08-30 under approval number K160149. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Miret Grasper, Alligator, Miret Grasper, Maryland?

Miret Grasper, Alligator, Miret Grasper, Maryland is a medical device that received FDA 510(k) clearance on 2016-08-30. It is manufactured by Miret Surgical, Inc.. The 510(k) number is K160149.

When was Miret Grasper, Alligator, Miret Grasper, Maryland approved by the FDA?

Miret Grasper, Alligator, Miret Grasper, Maryland received FDA 510(k) clearance on 2016-08-30, under approval number K160149.

What company makes Miret Grasper, Alligator, Miret Grasper, Maryland?

Miret Grasper, Alligator, Miret Grasper, Maryland is manufactured by Miret Surgical, Inc..

What is the FDA product code for Miret Grasper, Alligator, Miret Grasper, Maryland?

The FDA product code for Miret Grasper, Alligator, Miret Grasper, Maryland is OCW.

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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.