FDA 510(k)

IMESH TACKER

K-Number: K110728 · 2011-06-08

Decision Date2011-06-08

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

IMESH TACKER is the device name listed in this FDA 510(k) record. The listed applicant is Easylap , Ltd.. It received FDA 510(k) clearance on 2011-06-08 under 510(k) number K110728. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMESH TACKER?

IMESH TACKER is a medical device that received FDA 510(k) clearance on 2011-06-08. The listed applicant is Easylap , Ltd.. The 510(k) number is K110728.

When did IMESH TACKER receive FDA 510(k) clearance?

IMESH TACKER received FDA 510(k) clearance on 2011-06-08, under 510(k) number K110728.

Who is the listed applicant for IMESH TACKER?

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

What is the FDA product code for IMESH TACKER?

The FDA product code for IMESH TACKER is GDW.

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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.