FDA 510(k)

LIPOCONTROL

K-Number: K090754 · 2011-01-21

Decision Date2011-01-21

Product CodeORK

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LIPOCONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Osyris Medical. It received FDA 510(k) clearance on 2011-01-21 under 510(k) number K090754. The device is classified under product code ORK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPOCONTROL?

LIPOCONTROL is a medical device that received FDA 510(k) clearance on 2011-01-21. The listed applicant is Osyris Medical. The 510(k) number is K090754.

When did LIPOCONTROL receive FDA 510(k) clearance?

LIPOCONTROL received FDA 510(k) clearance on 2011-01-21, under 510(k) number K090754.

Who is the listed applicant for LIPOCONTROL?

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

What is the FDA product code for LIPOCONTROL?

The FDA product code for LIPOCONTROL is ORK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.