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FDA 510(k)

No Stress Impress

K-Number: K213175 · 2023-01-19

Decision Date2023-01-19
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

No Stress Impress is a medical device manufactured by No Stress Impress, LLC. It received FDA 510(k) clearance on 2023-01-19 under approval number K213175. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the No Stress Impress?

No Stress Impress is a medical device that received FDA 510(k) clearance on 2023-01-19. It is manufactured by No Stress Impress, LLC. The 510(k) number is K213175.

When was No Stress Impress approved by the FDA?

No Stress Impress received FDA 510(k) clearance on 2023-01-19, under approval number K213175.

What company makes No Stress Impress?

No Stress Impress is manufactured by No Stress Impress, LLC.

What is the FDA product code for No Stress Impress?

The FDA product code for No Stress Impress is ELW.

Related Devices (Code: ELW)

Official Source

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