ClearanceBrief
Company ยท US

Kmi Kolster Methods, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2006. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GAWSuture, Nonabsorbable, Synthetic, Polypropylene2
FRNPump, Infusion1
IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat1
LHCWarmer, Irrigation Solution1
QPBSystem, Suction, Lipoplasty For Removal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 23, 2006K060414KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE
Kmi Kolster Methods, Inc.
GAW
Mar 4, 2005K043591FEATHERLIFT EXTENDED APTOS THREAD
Kmi Kolster Methods, Inc.
GAW
Nov 19, 2001K012236STARS2000 POWER CANNULA
Kmi Kolster Methods, Inc.
QPB
Aug 9, 2001K010702XUB EXTERNAL ULTRASOUND
Kmi Kolster Methods, Inc.
IMI
Nov 16, 2000K002859SSW-STERILE SOLUTION WARMER
Kmi Kolster Methods, Inc.
LHC
Oct 15, 1999K991203IRRIGATION OR INFUSION PUMP K PUMP
Kmi Kolster Methods, Inc.
FRN

Latest recalls

DateFirm and productCodeLinked 510(k)
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