Zymed Medical Instrumentation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zymed Medical Instrumentation - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Zymed Medical Instrumentation has 7 FDA 510(k) cleared medical devices. Based in Camarillo, US.
Historical record: 7 cleared submissions from 1993 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zymed Medical Instrumentation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zymed Medical Instrumentation
7 devices
Cleared
Sep 21, 2000
ZYBIT
Cardiovascular
80d
Cleared
Jul 28, 1999
MODIFICATION TO ZYMED HOLTER 2000
Cardiovascular
28d
Cleared
Apr 13, 1999
HOLTER 2000
Cardiovascular
84d
Cleared
Feb 16, 1999
ZYMED TELEMETRY SYSTEM, MODEL EASI VIEW
Cardiovascular
92d
Cleared
Mar 18, 1996
ZYMED HOLTER SCANNER MODEL 2010
Cardiovascular
138d
Cleared
Oct 06, 1995
ZYMED TELEMETRY SYSTEM
Cardiovascular
193d
Cleared
Nov 01, 1993
MULTITRAK-PLUS
Cardiovascular
252d