Lysonix Aspiration Pump

FDA 510(k) K980454 · Lysonix, Inc.

Substantially Equivalent

510(k) numberK980454

Submission

Device name
Lysonix Aspiration Pump
Applicant
Lysonix, Inc.
Carpinteria, CA, US
Received
February 5, 1998
Decision date
March 18, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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More from Shenzhen Kingboom Technology Co., Ltd.

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K980771Lysonix Suction Lipoplasty SystemQPB · Traditional 07/13/1998SE
K980763Lysonix Lipoplasty Access PortQPB · Traditional 05/28/1998SE
K974233Lysonix Irrigation SystemGBX · Traditional 02/03/1998SE
K972958Lysonix TTD Delta Scavenger Suction/Aspiration Cannulas Lysonix Infusion Diamond CannulasGCJ · Traditional 09/19/1997SE

Questions and answers

When was Lysonix Aspiration Pump cleared by the FDA?

Lysonix Aspiration Pump (K980454) received a 510(k) decision of Substantially Equivalent on March 18, 1998, 41 days after the submission was received.

What is the product code of K980454?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.