DEVICE, PERCUTANEOUS, BIOPSY
FDA product code MJG · Class 1 · 16 devices · 15 reports · 9 devices named in recalls
- Cook G00012Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall2 reports
- Cook G00013Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G00850Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G00852Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G01559Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G03314Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G03978Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G04338Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- Cook G05040Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 recall0 reports
- NA 03.804.517SSynthes GmbH · DEVICE, PERCUTANEOUS, BIOPSY7 reports
- Kyphon V Premium Vertebroplasty VPB13Medtronic Sofamor Danek, Inc. · DEVICE, PERCUTANEOUS, BIOPSY1 report
- Cook G00810Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 report
- Cook G00895Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 report
- Cook G01047Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 report
- Greene G03383Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 report
- Cook G03954Cook Incorporated · DEVICE, PERCUTANEOUS, BIOPSY1 report