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FDA 510(k)

MACROPORE PURICEL LIPOPLASTY SYSTEM

K-Number: K042261 · 2004-09-20

ApplicantMacropore Biosurgery, Inc.
Decision Date2004-09-20
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MACROPORE PURICEL LIPOPLASTY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Macropore Biosurgery, Inc.. It received FDA 510(k) clearance on 2004-09-20 under 510(k) number K042261. 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 MACROPORE PURICEL LIPOPLASTY SYSTEM?

MACROPORE PURICEL LIPOPLASTY SYSTEM is a medical device that received FDA 510(k) clearance on 2004-09-20. The listed applicant is Macropore Biosurgery, Inc.. The 510(k) number is K042261.

When did MACROPORE PURICEL LIPOPLASTY SYSTEM receive FDA 510(k) clearance?

MACROPORE PURICEL LIPOPLASTY SYSTEM received FDA 510(k) clearance on 2004-09-20, under 510(k) number K042261.

Who is the listed applicant for MACROPORE PURICEL LIPOPLASTY SYSTEM?

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

What is the FDA product code for MACROPORE PURICEL LIPOPLASTY SYSTEM?

The FDA product code for MACROPORE PURICEL LIPOPLASTY SYSTEM is QPB.

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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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