Company ยท US
Oec-Diasonics, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1993. Name variants (Inc, Corp, punctuation) are merged.
8510(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 21, 1993 | K926056 | 9600 FLUOROSCOPIC IMAGING SYSTEM Oec-Diasonics, Inc. | OXO |
| Jan 4, 1993 | K924879 | EP 3000 Oec-Diasonics, Inc. | JAA |
| Jan 10, 1992 | K914446 | UROVIEW 2000, MODIFICATION Oec-Diasonics, Inc. | JAA |
| Mar 1, 1990 | K896583 | F.A.S.T. TABLE Oec-Diasonics, Inc. | IXR |
| Aug 10, 1989 | K893475 | UROVIEW II Oec-Diasonics, Inc. | JAA |
| Jul 16, 1987 | K872022 | UROVIEW Oec-Diasonics, Inc. | KQS |
| Jan 30, 1987 | K864837 | MODIFIED MAINFRAME OF MODEL 902 MOBILE C-ARM Oec-Diasonics, Inc. | JAA |
| Jan 3, 1985 | K843972 | ANGIOPLUS-S Oec-Diasonics, Inc. | JAA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||