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FDA 510(k)

LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE

K-Number: K010311 · 2001-06-29

ApplicantEuromi S.A
Decision Date2001-06-29
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Euromi S.A. It received FDA 510(k) clearance on 2001-06-29 under 510(k) number K010311. 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 LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE?

LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE is a medical device that received FDA 510(k) clearance on 2001-06-29. The listed applicant is Euromi S.A. The 510(k) number is K010311.

When did LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE receive FDA 510(k) clearance?

LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE received FDA 510(k) clearance on 2001-06-29, under 510(k) number K010311.

Who is the listed applicant for LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE?

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

What is the FDA product code for LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE?

The FDA product code for LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE 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 Euromi S.A 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.

K101413EUROMI EVA SP6

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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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