Gyrus Medical, Inc
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| GYRUS ACMI, REF 3345 -Everest BiCOAG MOLly Forceps 5mm/45cm REF 3345PK - PKS MOLly Forceps recall (Z-0100-2015) | Gyrus Medical, Inc | 2014-10-21 |
| Gyrus ACMI Falope-Ring Dilator, item 000878-4. The Falope-Ring Dilator is a conical plasti recall (Z-2269-2014) | Gyrus Medical, Inc | 2014-08-19 |
| Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. REF 006889-901 and REF 005280-901 recall (Z-1196-2014) | Gyrus Medical, Inc | 2014-03-13 |
| GYRUS ACMI, REF 3740, Everest BiCOAG Bipolar Dissecting Forceps 5mm/45 cm, Sterile EO. GYR recall (Z-1983-2013) | Gyrus Medical, Inc | 2013-08-19 |
| GYRUS ACMI PKS PlasmaSEAL Open Forceps, model 2103PK and 917015PK. Sterile EO. The device recall (Z-1175-06) | Gyrus Medical, Inc. | 2006-06-27 |
| Gyrus PlasmaKinetic Super Pulse Generator is a micro-computer based radio frequency genera recall (Z-0841-04) | Gyrus Medical, Inc | 2004-07-20 |
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Every clearance here is in the API, with alerts when new ones post.