Company ยท US
Sienco, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2023. Name variants (Inc, Corp, punctuation) are merged.
5510(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 4, 2023 | K223635 | Sonoclot Coagulation & Platelet Function Analyzer System with Sonoclot Viewer Sienco, Inc. | JBP |
| Dec 12, 2003 | K032952 | AIACT KIT Sienco, Inc. | JBP |
| Aug 31, 2000 | K002528 | SONOCLOT COAGULATION & PLATELET FUNCTION ANALYZER SYSTEM WITH SIGNATURE VIEWER OPTION Sienco, Inc. | JBP |
| May 28, 1999 | K984141 | GBACT + KIT Sienco, Inc. | JBP |
| Sep 5, 1995 | K952560 | SONOCLOT COAGULATION & PLATELET FUNCTION ANALYZER Sienco, Inc. | JPA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||