Cellulize
K-Number: K180338 · 2018-09-21
ApplicantWard Photonics, LLC
Decision Date2018-09-21
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Cellulize is a medical device manufactured by Ward Photonics, LLC. It received FDA 510(k) clearance on 2018-09-21 under approval number K180338. 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 Cellulize?
Cellulize is a medical device that received FDA 510(k) clearance on 2018-09-21. It is manufactured by Ward Photonics, LLC. The 510(k) number is K180338.
When was Cellulize approved by the FDA?
Cellulize received FDA 510(k) clearance on 2018-09-21, under approval number K180338.
What company makes Cellulize?
Cellulize is manufactured by Ward Photonics, LLC.
What is the FDA product code for Cellulize?
The FDA product code for Cellulize 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.