FDA 510(k)

Pocket III

K-Number: K232302 · 2024-04-26

Decision Date2024-04-26

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Pocket III is the device name listed in this FDA 510(k) record. The listed applicant is Quantel Medical. It received FDA 510(k) clearance on 2024-04-26 under 510(k) 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. The listed applicant is Quantel Medical. The 510(k) number is K232302.

When did Pocket III receive FDA 510(k) clearance?

Pocket III received FDA 510(k) clearance on 2024-04-26, under 510(k) number K232302.

Who is the listed applicant for Pocket III?

The FDA 510(k) record lists Quantel Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pocket III?

The FDA product code for Pocket III is IYO.

Other records listing Quantel Medical 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.

K251507INTEGRE LIO K220430Capsulo K213254Axialis Ophthalmic Ultrasound System K201502Vitra 810 K191962Vitra 2 K183414ABSOLU

View all 9 devices →

Related Devices (Code: IYO)

K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApS K252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.K253714IntraSight PlusPhilips Image Guided Therapy Corporation

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.