Dms Products, Inc.
Dms Products, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 9, 1989.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K891004 | RAPIDEC STAPH | November 9, 1989 |
| K894805 | RAPIDEC UR | September 26, 1989 |
| K890626 | RAPIDEC COLI | June 2, 1989 |
| K890625 | JAMES REAGENT | February 17, 1989 |
| K854733 | API 20 EC (ENTEROBACTERIACEAE)(IDENTIFICATION KIT) | March 6, 1986 |
| K854732 | API 50 CHB (CULTURE MEDIA) | March 4, 1986 |