Lifestream Int'L, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Lifestream Int'L, Inc. has 23 FDA 510(k) cleared medical devices. Based in Sugar Land, US.
Historical record: 23 cleared submissions from 1984 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lifestream Int'L, Inc. Filter by specialty or product code using the sidebar.
23 devices
Cleared
Aug 08, 1997
VISION CARDIOPLEGIA DELIVERY SYSTEM
Cardiovascular
267d
Cleared
Sep 11, 1996
DIOMED 15, 30, 60 SURGICAL DIODE LASER
General & Plastic Surgery
85d
Cleared
May 13, 1993
CARDIOTOMY RESERVOIR W/20 MICRON FILITER
Cardiovascular
485d
Cleared
Mar 12, 1993
AUTOTRANSFUSION SUCTION SET
Anesthesiology
395d
Cleared
May 20, 1992
AUTOLOGOUS BLOOD PROCESSING SYSTEM
Anesthesiology
307d
Cleared
Dec 23, 1991
SURGI LIGHT NON-CONTACT FIBERS
General & Plastic Surgery
83d
Cleared
Oct 31, 1991
TMP PRESSURE ISOLATORR, TMP PRESSURE MONITOR SYST
Cardiovascular
176d
Cleared
Apr 22, 1991
MODIFICATION TO MODEL 90-1460 LASER ADAPTER
General & Plastic Surgery
18d
Cleared
Mar 29, 1991
LIGHT-TOUCH AND SURGI LIGHT FIBERS
General & Plastic Surgery
37d
Cleared
Feb 01, 1991
TMP LEFT ATRIAL PRESSURE CATH CAT.# 100-00X-000
Cardiovascular
122d
Cleared
Oct 26, 1990
SURGIMEDICS, SLP LAPAROSCOPIC CHOLANGIOGRAM CATH
General & Plastic Surgery
71d
Cleared
May 26, 1989
LIGHT-TOUCH/GS 905250 ND:YAG LASER MICRO PRO ENDOS
General & Plastic Surgery
60d