Smiths Medical
FDA Regulatory Profile
Smiths Medical appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 24, 2019.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K181660 | Acapella Choice Blue Vibratory PEP Device | October 24, 2019 |
| K050166 | PORTEX EMERGENCY CRICOTHYROIDOTOMY KIT | May 26, 2005 |
| K041348 | PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR | July 13, 2004 |