Lifestream Int'L, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Lifestream Int'L, Inc.
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