Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PiXel8-Reveal

K-Number: K233143 · 2024-02-02

Decision Date2024-02-02
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PiXel8-Reveal is a medical device manufactured by Rohrer Aesthetics. It received FDA 510(k) clearance on 2024-02-02 under approval number K233143. 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 PiXel8-Reveal?

PiXel8-Reveal is a medical device that received FDA 510(k) clearance on 2024-02-02. It is manufactured by Rohrer Aesthetics. The 510(k) number is K233143.

When was PiXel8-Reveal approved by the FDA?

PiXel8-Reveal received FDA 510(k) clearance on 2024-02-02, under approval number K233143.

What company makes PiXel8-Reveal?

PiXel8-Reveal is manufactured by Rohrer Aesthetics.

What is the FDA product code for PiXel8-Reveal?

The FDA product code for PiXel8-Reveal is GEX. This falls under the Gastroenterology category.

Other Devices by Rohrer Aesthetics

Related Devices (Code: GEX)

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.