Meridian Co., Ltd.
FDA Regulatory Profile
Meridian Co., Ltd. appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 1 compliance action on record. Its most recent 510(k) clearance was granted on February 25, 2011.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 1
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K102375 | LUCIA | February 25, 2011 |
| K081962 | LAPEX BCS | December 29, 2008 |
| K034009 | LAPEX 2000 | January 21, 2005 |
| K023238 | MCPULSE | February 19, 2003 |
| K020360 | ABR-2000 | August 29, 2002 |
| K010897 | MERIDIAN-PORTABLE | June 19, 2001 |
| K001347 | MERIDIAN-II AND MERDIAN-PLUS | November 3, 2000 |