ClearanceBrief
Company ยท US

Hemocleanse, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1999. 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
FLDApparatus, Hemoperfusion, Sorbent3
KNTTubes, Gastrointestinal (And Accessories)1
MLWWarmer, Peritoneal Dialysate1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 30, 1999K993330THERMOCHEM-HT SYSTEM
Hemocleanse, Inc.
MLW
Sep 10, 1999K992196BIOLOGIC-DT SYSTEM (BIOLOGIC-DT-1000 WITH DT-1000-TK)
Hemocleanse, Inc.
FLD
Aug 13, 1999K984546BIOLOGIC-DT MACHINE, MODEL DT-1000 AND BIOLOGIC-DT TREATMENT KIT, MODEL DT-1000-TK
Hemocleanse, Inc.
FLD
Feb 15, 1996K953751BIOLOGIC-DT SYSTEM
Hemocleanse, Inc.
FLD
Sep 30, 1994K923046BIOLOGIC DT-1000 MACHINE
Hemocleanse, Inc.
KNT

Latest recalls

DateFirm and productCodeLinked 510(k)
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