Dolphin Medical, Inc.
Dolphin Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2006.
Top product codes for Dolphin Medical, Inc.
Recent clearances by Dolphin Medical, Inc.
- K060524 — DOLPHIN 2000 DATEX COMPATIBLE OXIMETRY DISPOSABLE AND REUSABLE SENSORS AND EXTENSION CABLES
- K040380 — DOLPHIN MEDICAL DOLPHIN ONE ADULT REUSABLE FOREHEAD SENSOR, MODEL 420
- K033876 — DOLPHIN 2000 OXIMETRY SENSORS, MODELS 2020, 2040, 2060, 2070, 2321, 2323, 2341, 2342, 2343, 2344, 2220, 2260 AND 2422
- K032947 — NELLCOR COMPATIBLE DOLPHIN 2000 Y OXIMETRY SENSOR, MODEL 2210
- K031465 — MODEL 2100 PULSE OXIMETER
- K030629 — DOLPHIN MEDICAL 2150 HANDHELD PULSE OXIMETER
- K030952 — DOLPHIN 2000 PULSE OXIMETRY SENSORS MODELS 2010, 2311 ADULT, 2312 PEDIATRIC, 2313 INFANT, 2314 NEONATAL, 2421
- K024235 — DOLPHIN MEDICAL STAND-ALONE PULSE OXIMETER
- K014218 — OSI MEDICAL DIGITAL DOLPHIN 3000 PULSE OXIMETER; DIGITAL DOLPHIN REUSABLE OPTICAL SENSOR, MODEL 210'
- K021959 — DOLPHIN MEDICAL STAND-ALONE PULSE OXIMETER, MODEL 2100
- K012989 — DOLPHIN 2000 OXIMETRY SENSOR, MODELS, 2050, 2351, 2354, 2070
- K020075 — MODIFICATION TO OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.