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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 the device name listed in this FDA 510(k) record. The listed applicant is Biotex, Inc.. It received FDA 510(k) clearance on 2021-07-20 under 510(k) 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. The listed applicant is Biotex, Inc.. The 510(k) number is K203712.

When did The Slide receive FDA 510(k) clearance?

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

Who is the listed applicant for The Slide?

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

What is the FDA product code for The Slide?

The FDA product code for The Slide is LQZ.

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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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