Symbiosis Corp.
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Medi-Tech Magic Torque Glidex hydrophilic coated guidewire, .035 inch/180 cm and .035 inch recall (Z-0666-03) | Symbiosis Corp. | 2003-03-20 |
| Scimed ChoICE PT ''J'' Tip 182 cm Guide Wire, a single use, sterile (EO), device packaged recall (Z-0589-03) | Symbiosis Corp. | 2003-02-27 |
| Scimed ChoICE PT Extra Support PTCA Guide Wire with ICE Hydrophilic Coating, 300 cm length recall (Z-0590-03) | Symbiosis Corp. | 2003-02-27 |
| Scimed PT Graphix Intermediate PCTA Guide Wire with ICE Hydrophilic Coating, 300 cm length recall (Z-0591-03) | Symbiosis Corp. | 2003-02-27 |
| Product is a ChoICE 182 cm Guide Wire, intended to facilitate placement of balloon dilatat recall (Z-0592-03) | Symbiosis Corp. | 2003-02-27 |
| Boston Scientific Microvasive Radial Jaw 3 Single-Use Maximum Capacity Biopsy Forceps Need recall (Z-0562-03) | Symbiosis Corp. | 2003-02-21 |
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Every clearance here is in the API, with alerts when new ones post.