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FDA 510(k)

MultiPulse HoPLUS

K-Number: K231876 · 2024-02-22

ApplicantAsclepion Laser Technologies GmbH
Decision Date2024-02-22
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MultiPulse HoPLUS is the device name listed in this FDA 510(k) record. The listed applicant is Asclepion Laser Technologies GmbH. It received FDA 510(k) clearance on 2024-02-22 under 510(k) number K231876. 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 MultiPulse HoPLUS?

MultiPulse HoPLUS is a medical device that received FDA 510(k) clearance on 2024-02-22. The listed applicant is Asclepion Laser Technologies GmbH. The 510(k) number is K231876.

When did MultiPulse HoPLUS receive FDA 510(k) clearance?

MultiPulse HoPLUS received FDA 510(k) clearance on 2024-02-22, under 510(k) number K231876.

Who is the listed applicant for MultiPulse HoPLUS?

The FDA 510(k) record lists Asclepion Laser Technologies GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MultiPulse HoPLUS?

The FDA product code for MultiPulse HoPLUS is GEX. This falls under the Gastroenterology category.

Other records listing Asclepion Laser Technologies GmbH as applicant

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Related Devices (Code: GEX)

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.

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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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