Bentec Medical, Inc.
FDA Regulatory Profile
Bentec Medical, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 16, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K002650 | VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726 | February 16, 2001 |
| K971411 | DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SILICONE EPISTAXIS CATHETER KIT V-27030K | June 3, 1997 |
| K971517 | SILICONE PUTTY EAR PLUGS | June 2, 1997 |