Optus, Inc.
Optus, Inc. appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 2, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K945264 | OPTUS OTOSCOPES | February 2, 1996 |
| K953913 | OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIES | January 22, 1996 |
| K945268 | OPTUS BRONCHOSCOPES | December 21, 1995 |
| K945265 | OPTUS HYSTEROSCOPES AND CONTACT HYSTEROSCOPES | September 12, 1995 |
| K945262 | OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPES | May 26, 1995 |
| K945267 | OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPES | May 23, 1995 |
| K945266 | OPTUS LAPAROSCOPES AND OPERATING LAPAROSCOPES | February 23, 1995 |
| K944656 | OPTUS SINUSCOPES AND ACCESSORIES | January 26, 1995 |
| K945263 | OPTUS THORACOSCOPES | December 13, 1994 |
| K945269 | OPTUS LARYNGOSCOPES | November 7, 1994 |