Cellulize
K-Number: K180338 · 2018-09-21
Device Summary
Frequently Asked Questions
What is the Cellulize?
Cellulize is a medical device that received FDA 510(k) clearance on 2018-09-21. The listed applicant is Ward Photonics, LLC. The 510(k) number is K180338.
When did Cellulize receive FDA 510(k) clearance?
Cellulize received FDA 510(k) clearance on 2018-09-21, under 510(k) number K180338.
Who is the listed applicant for Cellulize?
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 Cellulize?
The FDA product code for Cellulize 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.
Related Devices (Code: OLI)
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.
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.