Zmi Corp.
Zmi Corp. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 14, 1992.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K915100 | BRINDLEY & SMITH ET-1000 | September 14, 1992 |
| K915159 | PEDIATRIC MULTI-FUNCTION ELECTRODES | February 7, 1992 |
| K913484 | ZOLL D-900 DEFIBRILLATOR | December 16, 1991 |
| K911956 | ZOLL PD-1400 PACER/DEFIBRILLATOR | July 31, 1991 |
| K895032 | ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES | October 12, 1989 |
| K885166 | ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODES | May 1, 1989 |
| K873402 | ZOLL NTP-1200 PACER/DEFIBRILLATOR | November 23, 1987 |
| K855015 | NONINVASIVE TEMP. PACEMAKER NTP-1000 | March 31, 1986 |