Careside, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Careside, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Careside, Inc. has 22 FDA 510(k) cleared chemistry devices. Based in Culver City, US.
Historical record: 22 cleared submissions from 1998 to 2002.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Careside, Inc.
22 devices
Cleared
Jul 03, 2002
CARESIDE LDH
Chemistry
140d
Cleared
Jul 01, 2002
CARESIDE GGT
Chemistry
138d
Cleared
Jun 04, 2002
CARESIDE ALT
Chemistry
111d
Cleared
Apr 15, 2002
CARESIDE TRGLYCERIDE
Chemistry
61d
Cleared
Nov 08, 2000
CARESIDE CHOLINESTERASE
Chemistry
62d
Cleared
Aug 21, 2000
CARESIDE HEMOGLOBIN
Hematology
103d
Cleared
Dec 27, 1999
CARESIDE DIRECT BILIRUBIN
Chemistry
49d
Cleared
Dec 02, 1999
CARESIDE ANALYZER
Chemistry
36d
Cleared
Sep 15, 1999
CARESIDE CO2, TOTAL
Chemistry
51d
Cleared
Aug 10, 1999
CARESIDE MG
Chemistry
82d
Cleared
Aug 03, 1999
CARESIDE AMMONIA
Chemistry
105d
Cleared
Jul 26, 1999
CARESIDE PT
Hematology
117d
Cleared
Apr 19, 1999
CARESIDE CKMB
Chemistry
67d
Cleared
Apr 19, 1999
CARESIDE CK
Chemistry
67d
Cleared
Mar 18, 1999
CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000
Chemistry
71d
Cleared
Mar 16, 1999
CARESIDE AST
Chemistry
71d
Cleared
Feb 08, 1999
CARESIDE AMYLASE
Chemistry
35d
Cleared
Jan 13, 1999
CARESIDE ALKALINE PHOSPHATASE
Chemistry
8d
Cleared
Dec 17, 1998
CARESIDE CALCIUM, ORIGINAL
Chemistry
51d
Cleared
Jun 25, 1998
CARESIDE URIC ACID
Chemistry
58d
Cleared
Jun 25, 1998
CARESIDE ANALYZER
Chemistry
56d
Cleared
Jun 23, 1998
CARESIDE TOTAL BILIRUBIN
Chemistry
50d