Lexa MINI (RIS-303, RIS-305)
K-Number: K233504 · 2024-02-08
Device Summary
Frequently Asked Questions
What is the Lexa MINI (RIS-303, RIS-305)?
Lexa MINI (RIS-303, RIS-305) is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is W&H Sterilization S.R.L.. The 510(k) number is K233504.
When did Lexa MINI (RIS-303, RIS-305) receive FDA 510(k) clearance?
Lexa MINI (RIS-303, RIS-305) received FDA 510(k) clearance on 2024-02-08, under 510(k) number K233504.
Who is the listed applicant for Lexa MINI (RIS-303, RIS-305)?
The FDA 510(k) record lists W&H Sterilization S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lexa MINI (RIS-303, RIS-305)?
The FDA product code for Lexa MINI (RIS-303, RIS-305) is FLE.
Other records listing W&H Sterilization S.R.L. 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: FLE)
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.