Company ยท US
Cambridge Bioscience Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 1989. 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 |
|---|---|---|---|
| Mar 15, 1989 | K890281 | HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES Cambridge Bioscience Corp. | LSR |
| Jul 8, 1988 | K881894 | ADENOCLONE(R)-TYPE 40/41 EIA DIAGNOSTIC TEST (48) Cambridge Bioscience Corp. | GOD |
| Feb 24, 1988 | K873312 | ADENOCLONE(TM)-IFA, ADENOVIRUS ANTIGEN TEST Cambridge Bioscience Corp. | GOD |
| Feb 24, 1988 | K873082 | ADENOCLONE(TM)-EIA ADENOVIRUS ANTIGEN TEST Cambridge Bioscience Corp. | GOD |
| Nov 5, 1985 | K852969 | ROTACLONE ROTAVIRUS DIAGNOSTIC KIT Cambridge Bioscience Corp. | LIQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||