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FDA 510(k)

I-LIPO SYSTEM

K-Number: K111501 · 2012-03-23

ApplicantChromogenex Technologies Limited
Decision Date2012-03-23
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

I-LIPO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Chromogenex Technologies Limited. It received FDA 510(k) clearance on 2012-03-23 under 510(k) number K111501. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I-LIPO SYSTEM?

I-LIPO SYSTEM is a medical device that received FDA 510(k) clearance on 2012-03-23. The listed applicant is Chromogenex Technologies Limited. The 510(k) number is K111501.

When did I-LIPO SYSTEM receive FDA 510(k) clearance?

I-LIPO SYSTEM received FDA 510(k) clearance on 2012-03-23, under 510(k) number K111501.

Who is the listed applicant for I-LIPO SYSTEM?

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

What is the FDA product code for I-LIPO SYSTEM?

The FDA product code for I-LIPO SYSTEM is OLI.

Related Clinical Trials

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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Other records listing Chromogenex Technologies Limited 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.

K081619CHROMOLITE EP

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Official Source

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