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FDA 510(k)

Resonic Rapid Acoustic Pulse Device

K-Number: K233804 · 2024-02-01

ApplicantZeltiq Aesthetics, Inc.
Decision Date2024-02-01
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Resonic Rapid Acoustic Pulse Device is a medical device manufactured by Zeltiq Aesthetics, Inc.. It received FDA 510(k) clearance on 2024-02-01 under approval number K233804. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Resonic Rapid Acoustic Pulse Device?

Resonic Rapid Acoustic Pulse Device is a medical device that received FDA 510(k) clearance on 2024-02-01. It is manufactured by Zeltiq Aesthetics, Inc.. The 510(k) number is K233804.

When was Resonic Rapid Acoustic Pulse Device approved by the FDA?

Resonic Rapid Acoustic Pulse Device received FDA 510(k) clearance on 2024-02-01, under approval number K233804.

What company makes Resonic Rapid Acoustic Pulse Device?

Resonic Rapid Acoustic Pulse Device is manufactured by Zeltiq Aesthetics, Inc..

What is the FDA product code for Resonic Rapid Acoustic Pulse Device?

The FDA product code for Resonic Rapid Acoustic Pulse Device is GEX. This falls under the Gastroenterology category.

Related Clinical Trials

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Related PubMed Literature

PMID: 41982627 Cybersecurity breaches in medical devices: analyzing FDA safety communications in response to patient security concerns. Frontiers in digital health (2026) PMID: 41815749 The history of state preemption and medical device regulation: lessons for artificial intelligence oversight. Health affairs scholar (2026) PMID: 40947420 Software as Medical Devices: requirements and regulatory landscape in the United States. Expert review of medical devices (2025) PMID: 40906998 Recalls of Arthroscopic Equipment After Food and Drug Administration 510(k) Approval: A Twenty-Year Analysis of Causes, Trends, and Time to Recall (2004 to 2024). The Journal of the American Academy of Orthopaedic Surgeons (2026)

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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.

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