Company ยท US
Ivd Research, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2009. 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 14, 2009 | K081064 | GIARDIA FECAL ANTIGEN DETECTION LATERAL FLOW KIT, MODEL GL-LF Ivd Research, Inc. | MHI |
| May 27, 2004 | K032897 | C. DIFFICILE TOXIN A + B FECAL ANTIGEN DETECTION MICROWELL ELISA KIT MODEL; CDIFF-96 Ivd Research, Inc. | LLH |
| Jul 10, 2003 | K031059 | IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96 Ivd Research, Inc. | MHJ |
| Mar 5, 2003 | K024113 | IVD CRYPTO/GIARDIA DFA Ivd Research, Inc. | MHI |
| Sep 17, 2002 | K020583 | IVD GIARDIA ANTIGEN DETECTION ASSAY MODEL GL-96 Ivd Research, Inc. | MHI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||