Envitec-Wismar GmbH
Envitec-Wismar GmbH holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2014.
Top product codes for Envitec-Wismar GmbH
Recent clearances by Envitec-Wismar GmbH
- K133064 — MYSIGN S PULSE OXIMETER, MYSIGN PC SOFTWARE (OPTIONAL), SOFTTIP LARGE R-3211-31, FINGER CLIP F-3211-31
- K122290 — ENVITEC MYSIGN O OXYGEN MEASURING DEVICE
- K102270 — ENVITEC REUSABLE SPO2 SENSORS TYPE NIHON-KOHDEN
- K090438 — REUSABLE ENVITEC FINGER SPO2 SENSOR-HP/PHILIPS COMPATIBLE, MODELS F-2412, F-2414-15, REUSABLE ENVITEC EAR SPO2 SENSOR
- K082655 — ENVITEC MEDICAL OXYGEN SENORS, MODELS OOM101; 00M102/-1; OOM103/-1/-1M; OOM104; OOM105; 00M106
- K070193 — ENVITEC OXIPEN PULSE OXIMETER AND ACCESSORIES
- K060675 — ENVITEC REUSABLE SOFTIP Y SPO2 SENSORS
- K043463 — ENVITEC REUSABLE MULTI-SITE Y SPO2 SENSORS
- K992215 — MULTICOMPATIBLE ENVITEC FINGER CLIP SENSOR, MULTICOMPATIBLE ENVITEC ADULT DISPOSABLE SENSOR, MULTICOMPATIBLE ENVITEC PED
Data sourced from openFDA. This site is unofficial and independent of the FDA.