Northgate Technologies, Inc.
4 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the recall (Z-1883-2020) | Northgate Technologies, Inc. | 2020-03-24 |
| AUTOLITH URO-TCH 9FR PROBE 54CM; NTI Catalog Number 9-203-0543 - Product Usage: Probes are recall (Z-1884-2020) | Northgate Technologies, Inc. | 2020-03-24 |
| ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies, America (OSTA); NTI recall (Z-1885-2020) | Northgate Technologies, Inc. | 2020-03-24 |
| Olympus Fluid Aspiration Set; a sterile set of silicone tubing and connectors for use with recall (Z-3179-2011) | Northgate Technologies, Inc. | 2011-09-09 |
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Every clearance here is in the API, with alerts when new ones post.