David Simmonds Co., Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K822848 | PRIMARY & SECONDARY I.V. TUBING SETS | October 15, 1982 |
| K820574 | ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL | March 23, 1982 |
| K820527 | ANESTHESIA EXTENSION TUBES | March 18, 1982 |