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FDA 510(k)

ENSEAL X1 Large Jaw Tissue Sealer

K-Number: K163548 · 2017-02-14

Decision Date2017-02-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENSEAL X1 Large Jaw Tissue Sealer is a medical device manufactured by Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2017-02-14 under approval number K163548. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENSEAL X1 Large Jaw Tissue Sealer?

ENSEAL X1 Large Jaw Tissue Sealer is a medical device that received FDA 510(k) clearance on 2017-02-14. It is manufactured by Ethicon Endo-Surgery, LLC. The 510(k) number is K163548.

When was ENSEAL X1 Large Jaw Tissue Sealer approved by the FDA?

ENSEAL X1 Large Jaw Tissue Sealer received FDA 510(k) clearance on 2017-02-14, under approval number K163548.

What company makes ENSEAL X1 Large Jaw Tissue Sealer?

ENSEAL X1 Large Jaw Tissue Sealer is manufactured by Ethicon Endo-Surgery, LLC.

What is the FDA product code for ENSEAL X1 Large Jaw Tissue Sealer?

The FDA product code for ENSEAL X1 Large Jaw Tissue Sealer is GEI.

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Official Source

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