Cambridge Bioscience Corp.
Cambridge Bioscience Corp. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 15, 1989.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K890281 | HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES | March 15, 1989 |
| K881894 | ADENOCLONE(R)-TYPE 40/41 EIA DIAGNOSTIC TEST (48) | July 8, 1988 |
| K873082 | ADENOCLONE(TM)-EIA ADENOVIRUS ANTIGEN TEST | February 24, 1988 |
| K873312 | ADENOCLONE(TM)-IFA, ADENOVIRUS ANTIGEN TEST | February 24, 1988 |
| K852969 | ROTACLONE ROTAVIRUS DIAGNOSTIC KIT | November 5, 1985 |