Kmb Medical Products Co.
Kmb Medical Products Co. appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 26, 1988.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K880850 | KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE | May 26, 1988 |