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FDA 510(k)

Miret Grasper, Alligator, Miret Grasper, Maryland

K-Number: K160149 · 2016-08-30

ApplicantMiret Surgical, Inc.
Decision Date2016-08-30
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Miret Grasper, Alligator, Miret Grasper, Maryland is the device name listed in this FDA 510(k) record. The listed applicant is Miret Surgical, Inc.. It received FDA 510(k) clearance on 2016-08-30 under 510(k) 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. The listed applicant is Miret Surgical, Inc.. The 510(k) number is K160149.

When did Miret Grasper, Alligator, Miret Grasper, Maryland receive FDA 510(k) clearance?

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

Who is the listed applicant for Miret Grasper, Alligator, Miret Grasper, Maryland?

The FDA 510(k) record lists Miret Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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