Medi-Globe Corporation
Medi-Globe Corporation holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2016.
Top product codes for Medi-Globe Corporation
Recent clearances by Medi-Globe Corporation
- K153264 — EasyPass Guidewire
- K142258 — PolyCatch Retrieval Device
- K133763 — SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM
- K091257 — MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM
- K083802 — SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025
- K070129 — SONOTIP II ULTRASOUND NEEDLE SYSTEM
- K061684 — MEDI-GLOBE ROTA-CUT SPHINCTEROTOME
Data sourced from openFDA. This site is unofficial and independent of the FDA.