ClearanceBrief
Company ยท US

Lysonix, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 1998. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QPBSystem, Suction, Lipoplasty For Removal2
BTAPump, Portable, Aspiration (Manual Or Powered)1
GBXCatheter, Irrigation1
GCJLaparoscope, General & Plastic Surgery1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 13, 1998K980771LYSONIX SUCTION LIPOPLASTY SYSTEM
Lysonix, Inc.
QPB
May 28, 1998K980763LYSONIX LIPOPLASTY ACCESS PORT
Lysonix, Inc.
QPB
Mar 18, 1998K980454LYSONIX ASPIRATION PUMP
Lysonix, Inc.
BTA
Feb 3, 1998K974233LYSONIX IRRIGATION SYSTEM
Lysonix, Inc.
GBX
Sep 19, 1997K972958LYSONIX TTD DELTA SCAVENGER SUCTION/ASPIRATION CANNULAS LYSONIX INFUSION DIAMOND CANNULAS
Lysonix, Inc.
GCJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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