Aid-U
K-Number: K231662 · 2024-02-08
ApplicantIaid
Decision Date2024-02-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Aid-U is the device name listed in this FDA 510(k) record. The listed applicant is Iaid. It received FDA 510(k) clearance on 2024-02-08 under 510(k) number K231662. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aid-U?
Aid-U is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is Iaid. The 510(k) number is K231662.
When did Aid-U receive FDA 510(k) clearance?
Aid-U received FDA 510(k) clearance on 2024-02-08, under 510(k) number K231662.
Who is the listed applicant for Aid-U?
The FDA 510(k) record lists Iaid as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aid-U?
The FDA product code for Aid-U is LLZ.
Related Devices (Code: LLZ)
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
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