Optus, Inc.
Optus, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1996.
Top product codes for Optus, Inc.
Recent clearances by Optus, Inc.
- K945264 — OPTUS OTOSCOPES
- K953913 — OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIES
- K945268 — OPTUS BRONCHOSCOPES
- K945265 — OPTUS HYSTEROSCOPES AND CONTACT HYSTEROSCOPES
- K945262 — OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPES
- K945267 — OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPES
- K945266 — OPTUS LAPAROSCOPES AND OPERATING LAPAROSCOPES
- K944656 — OPTUS SINUSCOPES AND ACCESSORIES
- K945263 — OPTUS THORACOSCOPES
- K945269 — OPTUS LARYNGOSCOPES
Data sourced from openFDA. This site is unofficial and independent of the FDA.