Epilaser Pro
K-Number: K233224 · 2024-01-27
Device Summary
Frequently Asked Questions
What is the Epilaser Pro?
Epilaser Pro is a medical device that received FDA 510(k) clearance on 2024-01-27. The listed applicant is Epilady 2000, LLC. The 510(k) number is K233224.
When did Epilaser Pro receive FDA 510(k) clearance?
Epilaser Pro received FDA 510(k) clearance on 2024-01-27, under 510(k) number K233224.
Who is the listed applicant for Epilaser Pro?
The FDA 510(k) record lists Epilady 2000, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Epilaser Pro?
The FDA product code for Epilaser Pro is GEX. This falls under the Gastroenterology category.
Other records listing Epilady 2000, 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: GEX)
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.