Suzuken Co., Ltd.
Suzuken Co., Ltd. appears in FDA public data with 0 recalls, 13 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 1, 2018.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K172068 | Kenz Cardico1211 | Jun 1, 2018 |
| K101024 | KENZ CARDY302 MAX | Jan 6, 2011 |
| K092389 | DISPOSAL ECG ELECTRODES, MODEL EASYRODE | Oct 13, 2009 |
| K001896 | KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTRO | Jan 8, 2001 |
| K870443 | KENZ-CARDICO 1201 | Jul 1, 1987 |
| K862544 | KENZ-ECG-102 SINGLE CHANNEL ELECTROCARDIOGRAPH | Aug 6, 1986 |
| K843731 | KENZ 80Z MARK II | Jul 11, 1985 |
| K822968 | ELECTROCARDIOGRAPH INTERPRETER | Dec 15, 1982 |
| K820854 | KENZ-45M | Jun 1, 1982 |
| K820991 | KENZ-GELECT GEL PAD | Apr 26, 1982 |
| K812263 | KENZ-GELECT | Nov 2, 1981 |
| K811949 | KENL-ECG-3 | Aug 13, 1981 |
| K811950 | KENL-ECG | Aug 13, 1981 |