Stephens Instruments
Stephens Instruments appears in FDA public data with 0 recalls, 5 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 1, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K022842 | STEPHENS DISPOSABLE HOOKS | November 1, 2002 |
| K022840 | STEPHENS DISPOSABLE SCISSORS | November 1, 2002 |
| K022835 | STEPHENS DISPOSABLE FORCEPS | November 1, 2002 |
| K022836 | STEPHENS DISPOSABLE SPECULUM | November 1, 2002 |
| K022843 | GAYHEART CORNEAL EXCISION DEVICE | November 1, 2002 |