Zmi Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zmi Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Zmi Corp. has 8 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Historical record: 8 cleared submissions from 1986 to 1992. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zmi Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zmi Corp.
8 devices
Cleared
Sep 14, 1992
BRINDLEY & SMITH ET-1000
Neurology
307d
Cleared
Feb 07, 1992
PEDIATRIC MULTI-FUNCTION ELECTRODES
Cardiovascular
85d
Cleared
Dec 16, 1991
ZOLL D-900 DEFIBRILLATOR
Cardiovascular
132d
Cleared
Jul 31, 1991
ZOLL PD-1400 PACER/DEFIBRILLATOR
Cardiovascular
90d
Cleared
Oct 12, 1989
ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES
Cardiovascular
65d
Cleared
May 01, 1989
ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODES
Cardiovascular
139d
Cleared
Nov 23, 1987
ZOLL NTP-1200 PACER/DEFIBRILLATOR
Cardiovascular
91d
Cleared
Mar 31, 1986
NONINVASIVE TEMP. PACEMAKER NTP-1000
Cardiovascular
105d