ClearanceBrief
Company ยท US

Klein-Baker Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 1997. 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
FOSCatheter, Umbilical Artery1
FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1
KDJSet, Administration, For Peritoneal Dialysis, Disposable1
LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days1
MIANeedle, Spinal, Short Term1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 29, 1997K972731NEO-CARE PERITONEAL DIALYSIS ADMINISTRATION SET
Klein-Baker Medical, Inc.
KDJ
May 22, 1997K970997NEO-CARE LUMBER PUNCTURE KIT
Klein-Baker Medical, Inc.
MIA
Apr 1, 1997K970434NEO-PICC
Klein-Baker Medical, Inc.
LJS
Dec 24, 1996K963972NEO-CARE DUAL LUMEN UMBILICAL CATHETER
Klein-Baker Medical, Inc.
FOS
Nov 6, 1996K963867NEO-CARE CATHETERIZATION TRAY
Klein-Baker Medical, Inc.
FOZ

Latest recalls

DateFirm and productCodeLinked 510(k)
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