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FDA 510(k)

UltraSlim Digital, UltraSmooth Digital

K-Number: K202361 · 2020-12-18

ApplicantWard Photonics, LLC
Decision Date2020-12-18
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UltraSlim Digital, UltraSmooth Digital is the device name listed in this FDA 510(k) record. The listed applicant is Ward Photonics, LLC. It received FDA 510(k) clearance on 2020-12-18 under 510(k) number K202361. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UltraSlim Digital, UltraSmooth Digital?

UltraSlim Digital, UltraSmooth Digital is a medical device that received FDA 510(k) clearance on 2020-12-18. The listed applicant is Ward Photonics, LLC. The 510(k) number is K202361.

When did UltraSlim Digital, UltraSmooth Digital receive FDA 510(k) clearance?

UltraSlim Digital, UltraSmooth Digital received FDA 510(k) clearance on 2020-12-18, under 510(k) number K202361.

Who is the listed applicant for UltraSlim Digital, UltraSmooth Digital?

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

What is the FDA product code for UltraSlim Digital, UltraSmooth Digital?

The FDA product code for UltraSlim Digital, UltraSmooth Digital is OLI.

Other records listing Ward Photonics, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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