Haemoscope Corp.
Haemoscope Corp. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 31, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K062604 | RAPIDTEG TEG-ACT TEST | January 31, 2007 |
| K041502 | THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY | September 1, 2004 |
| K002177 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES | September 14, 2000 |
| K993678 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIES | May 5, 2000 |
| K954437 | THROMBELASTOGRAPH COAGULATION ANALYZER 3000S | January 30, 1996 |
| K904204 | THROMBELASTOGRAPH | November 1, 1990 |
| K895844 | THROMBELASTOGRAPH(R) | October 24, 1989 |