Physician Industries, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K040565 | PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE | July 22, 2004 |
| K033739 | PHYSICIAN INDUSTRIES' DURAMETER SYRINGE | July 12, 2004 |
| K960248 | GENERAL PROCEDURE KIT | April 12, 1996 |
| K954068 | GENERAL HYGIENE KIT | November 8, 1995 |