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FDA 510(k)

LIPOSE DISPOSABLE CANNULA

K-Number: K093067 · 2009-12-29

ApplicantLipose Corp.
Decision Date2009-12-29
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIPOSE DISPOSABLE CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Lipose Corp.. It received FDA 510(k) clearance on 2009-12-29 under 510(k) number K093067. 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 LIPOSE DISPOSABLE CANNULA?

LIPOSE DISPOSABLE CANNULA is a medical device that received FDA 510(k) clearance on 2009-12-29. The listed applicant is Lipose Corp.. The 510(k) number is K093067.

When did LIPOSE DISPOSABLE CANNULA receive FDA 510(k) clearance?

LIPOSE DISPOSABLE CANNULA received FDA 510(k) clearance on 2009-12-29, under 510(k) number K093067.

Who is the listed applicant for LIPOSE DISPOSABLE CANNULA?

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

What is the FDA product code for LIPOSE DISPOSABLE CANNULA?

The FDA product code for LIPOSE DISPOSABLE CANNULA is QPB.

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 Lipose Corp. 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.

K081848LIPOSE FAT TRANSFER SYSTEM

Related Devices (Code: QPB)

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

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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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