Photonica Professional
K-Number: K160880 · 2016-09-23
ApplicantWard Photonics, LLC
Decision Date2016-09-23
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Photonica Professional is a medical device manufactured by Ward Photonics, LLC. It received FDA 510(k) clearance on 2016-09-23 under approval number K160880. 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 Photonica Professional?
Photonica Professional is a medical device that received FDA 510(k) clearance on 2016-09-23. It is manufactured by Ward Photonics, LLC. The 510(k) number is K160880.
When was Photonica Professional approved by the FDA?
Photonica Professional received FDA 510(k) clearance on 2016-09-23, under approval number K160880.
What company makes Photonica Professional?
Photonica Professional is manufactured by Ward Photonics, LLC.
What is the FDA product code for Photonica Professional?
The FDA product code for Photonica Professional 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.