MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE — Abbott Laboratories (510(k) K001616)
MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE — Abbott Laboratories (510(k) K001616) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE; Applicant: Abbott Laboratories; Clearance track: 510(k).
| Device name | MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE |
|---|---|
| Applicant | Abbott Laboratories |
| Clearance track | 510(k) |
| Submission number | K001616 |
| Decision | Substantially Equivalent |
| Decision date | 2000-07-27 |
| Date received | 2000-05-25 |
| Product code | FOZ |
| Device class | 2 |
| Medical specialty | General Hospital |
| Applicant location | IL, US |
| Source | openFDA device |
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