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FDA 510(k)

ERCHONIA IOTO_240

K-Number: K062792 · 2007-03-01

ApplicantErchonia Medical, Inc.
Decision Date2007-03-01
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ERCHONIA IOTO_240 is the device name listed in this FDA 510(k) record. The listed applicant is Erchonia Medical, Inc.. It received FDA 510(k) clearance on 2007-03-01 under 510(k) number K062792. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERCHONIA IOTO_240?

ERCHONIA IOTO_240 is a medical device that received FDA 510(k) clearance on 2007-03-01. The listed applicant is Erchonia Medical, Inc.. The 510(k) number is K062792.

When did ERCHONIA IOTO_240 receive FDA 510(k) clearance?

ERCHONIA IOTO_240 received FDA 510(k) clearance on 2007-03-01, under 510(k) number K062792.

Who is the listed applicant for ERCHONIA IOTO_240?

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

What is the FDA product code for ERCHONIA IOTO_240?

The FDA product code for ERCHONIA IOTO_240 is EGJ.

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Other records listing Erchonia Medical, Inc. as applicant

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Related Devices (Code: EGJ)

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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