K842685 is an FDA 510(k) clearance for the BECTON DICKINSON 1000 INSULIN PUMP..
Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on July 10, 1984.
This device falls under the General Hospital FDA review panel.
| 510(k) Number | K842685 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Product Development Protocol (SESP) |
| Date Received | July 10, 1984 |
| Decision Date | July 10, 1984 |
| Days to Decision | — |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | — |
| Product Code | — |
| Device Class | — |