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 a medical device manufactured by Ward Photonics, LLC. It received FDA 510(k) clearance on 2020-12-18 under approval 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. It is manufactured by Ward Photonics, LLC. The 510(k) number is K202361.
When was UltraSlim Digital, UltraSmooth Digital approved by the FDA?
UltraSlim Digital, UltraSmooth Digital received FDA 510(k) clearance on 2020-12-18, under approval number K202361.
What company makes UltraSlim Digital, UltraSmooth Digital?
UltraSlim Digital, UltraSmooth Digital is manufactured by Ward Photonics, LLC.
What is the FDA product code for UltraSlim Digital, UltraSmooth Digital?
The FDA product code for UltraSlim Digital, UltraSmooth Digital is OLI.
Other Devices by Ward Photonics, LLC
Related Devices (Code: OLI)
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.