ClearanceBrief
Company ยท US

Zmi Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1992. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DROPacemaker, Cardiac, External Transcutaneous (Non-Invasive)4
LDDDc-Defibrillator, Low-Energy, (Including Paddles)2
DRFCatheter, Electrode Recording, Or Probe, Electrode Recording1
LIHInterferential Current Therapy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 14, 1992K915100BRINDLEY & SMITH ET-1000
Zmi Corp., HK
LIH
Feb 7, 1992K915159PEDIATRIC MULTI-FUNCTION ELECTRODES
Zmi Corp.
DRF
Dec 16, 1991K913484ZOLL D-900 DEFIBRILLATOR
Zmi Corp.
LDD
Jul 31, 1991K911956ZOLL PD-1400 PACER/DEFIBRILLATOR
Zmi Corp.
DRO
Oct 12, 1989K895032ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES
Zmi Corp.
LDD
May 1, 1989K885166ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODES
Zmi Corp.
DRO
Nov 23, 1987K873402ZOLL NTP-1200 PACER/DEFIBRILLATOR
Zmi Corp.
DRO
Mar 31, 1986K855015NONINVASIVE TEMP. PACEMAKER NTP-1000
Zmi Corp.
DRO

Latest recalls

DateFirm and productCodeLinked 510(k)
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