Aspen Labs
Aspen Labs appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 30, 1997.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K970493 | HYFRECATOR 2000 | April 30, 1997 |
| K925333 | SINGLE USE TUNGSTEN WIRE LEE LOOP ELECTRODE | September 27, 1994 |
| K931215 | HAND-TROL S | March 28, 1994 |
| K912046 | SINGLE USE LEE ELECTRODE | March 5, 1992 |
| K905654 | ELECTROSURGICAL UNIT WITH ACCESSORIES | March 18, 1991 |
| K904240 | SINGLE USE LAPARSCOPIC ELECTRODE | February 19, 1991 |