Pocket III
K-Number: K232302 · 2024-04-26
ApplicantQuantel Medical
Decision Date2024-04-26
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Pocket III is a medical device manufactured by Quantel Medical. It received FDA 510(k) clearance on 2024-04-26 under approval number K232302. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Pocket III?
Pocket III is a medical device that received FDA 510(k) clearance on 2024-04-26. It is manufactured by Quantel Medical. The 510(k) number is K232302.
When was Pocket III approved by the FDA?
Pocket III received FDA 510(k) clearance on 2024-04-26, under approval number K232302.
What company makes Pocket III?
Pocket III is manufactured by Quantel Medical.
What is the FDA product code for Pocket III?
The FDA product code for Pocket III is IYO.
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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.