Medi-Globe Corp.
Medi-Globe Corp. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2006.
Top product codes for Medi-Globe Corp.
Recent clearances by Medi-Globe Corp.
- K061222 — INJECTRA INJECTION NEEDLE
- K051247 — SONOTIP II ULTRASOUND NEEDLE SYSTEM
- K011261 — STONE EXTRACTOR BALLOON CATHETER
- K010714 — EXPANDER, MODELS 1400880, 1401280, 1401680, 1401880, 1410420, 1410620, 1410830
- K010549 — BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)
- K990220 — MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM
- K953355 — GIP/MEID-GLOBE HOT BIOPSY FORCEPS
- K955558 — GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES
- K953827 — GIP/MEDI-GLOBE ERCP CATHETERS
- K941973 — GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES
- K943629 — GIP/MEDI-GLOBE PAPILLOTOME
- K943935 — GIP/MEDI-GLOBE POLYPECTOMY SNARES
- K935844 — GIP/MEDI-GLOBE NEEDLE SYSTEM FOR ULTRASONIC FNA
- K943476 — GIP/MEDI-GLOBE GOREIGN BODY GRASPERS
- K942005 — GIP/MED-GLOBE STONE EXTRACTOR BASKETS
- K942544 — GIP/MEDI-GLOBE MECHANICAL LITHOTRIPTOR AND BASKETS
- K941359 — GIP/MEDI-GLOBE BIOPSY FORCEPS
- K900459 — APPLICARD (EKG)
Data sourced from openFDA. This site is unofficial and independent of the FDA.