Vomed Volzer Medizintechnik GmbH & Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K023019 | VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000 | December 10, 2002 |
| K022257 | VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006 XXX-9011 XXX | October 4, 2002 |
| K022318 | VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES | September 19, 2002 |