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FDA 510(k)

AIRBRUSH LIPOSCULPTOR SYSTEM

K-Number: K031881 · 2003-07-28

ApplicantBiosculpture Technology, Inc.
Decision Date2003-07-28
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AIRBRUSH LIPOSCULPTOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biosculpture Technology, Inc.. It received FDA 510(k) clearance on 2003-07-28 under 510(k) number K031881. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRBRUSH LIPOSCULPTOR SYSTEM?

AIRBRUSH LIPOSCULPTOR SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-28. The listed applicant is Biosculpture Technology, Inc.. The 510(k) number is K031881.

When did AIRBRUSH LIPOSCULPTOR SYSTEM receive FDA 510(k) clearance?

AIRBRUSH LIPOSCULPTOR SYSTEM received FDA 510(k) clearance on 2003-07-28, under 510(k) number K031881.

Who is the listed applicant for AIRBRUSH LIPOSCULPTOR SYSTEM?

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

What is the FDA product code for AIRBRUSH LIPOSCULPTOR SYSTEM?

The FDA product code for AIRBRUSH LIPOSCULPTOR SYSTEM is QPB.

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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.

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