Home use hair removal device, model: Precise Touch Pro
K-Number: K213830 · 2022-02-01
Device Summary
Frequently Asked Questions
What is the Home use hair removal device, model: Precise Touch Pro?
Home use hair removal device, model: Precise Touch Pro is a medical device that received FDA 510(k) clearance on 2022-02-01. The listed applicant is Iluminage Beauty Co., Limited. The 510(k) number is K213830.
When did Home use hair removal device, model: Precise Touch Pro receive FDA 510(k) clearance?
Home use hair removal device, model: Precise Touch Pro received FDA 510(k) clearance on 2022-02-01, under 510(k) number K213830.
Who is the listed applicant for Home use hair removal device, model: Precise Touch Pro?
The FDA 510(k) record lists Iluminage Beauty Co., Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Home use hair removal device, model: Precise Touch Pro?
The FDA product code for Home use hair removal device, model: Precise Touch Pro is OHT.
Related Clinical Trials
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: OHT)
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.