Solaris Medical Technology, Inc.
Solaris Medical Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2010.
Top product codes for Solaris Medical Technology, Inc.
Recent clearances by Solaris Medical Technology, Inc.
- K100077 — NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103
- K101972 — SOLARIS REUSABLE AND DISPOSABLE BLOOD PRESSURE CUFFS
- K092950 — SOLARIS MODELS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
- K073249 — SOLARIS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES
- K061931 — SOLARIS COMPATIBLE REUSABLE ADULT SPO2 FINGER SENSORS, MODELS S100A-090103 AND 300103, S200A-090101 AND 300101
Data sourced from openFDA. This site is unofficial and independent of the FDA.