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FDA 510(k)

The Slide

K-Number: K203712 · 2021-07-20

ApplicantBiotex, Inc.
Decision Date2021-07-20
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

The Slide is a medical device manufactured by Biotex, Inc.. It received FDA 510(k) clearance on 2021-07-20 under approval number K203712. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the The Slide?

The Slide is a medical device that received FDA 510(k) clearance on 2021-07-20. It is manufactured by Biotex, Inc.. The 510(k) number is K203712.

When was The Slide approved by the FDA?

The Slide received FDA 510(k) clearance on 2021-07-20, under approval number K203712.

What company makes The Slide?

The Slide is manufactured by Biotex, Inc..

What is the FDA product code for The Slide?

The FDA product code for The Slide is LQZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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