Medi-Globe Corporation
Medi-Globe Corporation appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 19, 2016.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K153264 | EasyPass Guidewire | May 19, 2016 |
| K142258 | PolyCatch Retrieval Device | September 30, 2014 |
| K133763 | SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM | May 15, 2014 |
| K091257 | MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM | May 8, 2009 |
| K083802 | SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025 | March 20, 2009 |
| K070129 | SONOTIP II ULTRASOUND NEEDLE SYSTEM | January 31, 2007 |
| K061684 | MEDI-GLOBE ROTA-CUT SPHINCTEROTOME | June 27, 2006 |