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FDA 510(k)

LYSONIX SUCTION LIPOPLASTY SYSTEM

K-Number: K980771 · 1998-07-13

ApplicantLysonix, Inc.
Decision Date1998-07-13
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LYSONIX SUCTION LIPOPLASTY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lysonix, Inc.. It received FDA 510(k) clearance on 1998-07-13 under 510(k) number K980771. 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 LYSONIX SUCTION LIPOPLASTY SYSTEM?

LYSONIX SUCTION LIPOPLASTY SYSTEM is a medical device that received FDA 510(k) clearance on 1998-07-13. The listed applicant is Lysonix, Inc.. The 510(k) number is K980771.

When did LYSONIX SUCTION LIPOPLASTY SYSTEM receive FDA 510(k) clearance?

LYSONIX SUCTION LIPOPLASTY SYSTEM received FDA 510(k) clearance on 1998-07-13, under 510(k) number K980771.

Who is the listed applicant for LYSONIX SUCTION LIPOPLASTY SYSTEM?

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

What is the FDA product code for LYSONIX SUCTION LIPOPLASTY SYSTEM?

The FDA product code for LYSONIX SUCTION LIPOPLASTY SYSTEM is QPB.

Related Clinical Trials

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Other records listing Lysonix, Inc. 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.

K980763LYSONIX LIPOPLASTY ACCESS PORTK980454LYSONIX ASPIRATION PUMPK974233LYSONIX IRRIGATION SYSTEMK972958LYSONIX TTD DELTA SCAVENGER SUCTION/ASPIRATION CANNULAS LYSONIX INFUSION DIAMOND CANNULAS

Related Devices (Code: QPB)

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Official Source

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