Company ยท US
Haemoscope Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2007. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 31, 2007 | K062604 | RAPIDTEG TEG-ACT TEST Haemoscope Corp. | JBP |
| Sep 1, 2004 | K041502 | THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY Haemoscope Corp. | JOZ |
| Sep 14, 2000 | K002177 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES Haemoscope Corp. | JPA |
| May 5, 2000 | K993678 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIES Haemoscope Corp. | JPA |
| Jan 30, 1996 | K954437 | THROMBELASTOGRAPH COAGULATION ANALYZER 3000S Haemoscope Corp. | GKP |
| Nov 1, 1990 | K904204 | THROMBELASTOGRAPH Haemoscope Corp. | GKP |
| Oct 24, 1989 | K895844 | THROMBELASTOGRAPH(R) Haemoscope Corp. | GKP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||