Fischer Industries, 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 |
|---|
| K022154 | LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D | September 30, 2002 |
| K940112 | X-RAY FILM PROCESSOR | April 11, 1995 |
| K861837 | FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND | August 7, 1986 |