K896903 is an FDA 510(k) clearance for the FIRST MEDIC MODEL 510. This device is classified as a Dc-defibrillator, Low-energy, (including Paddles) (Class II - Special Controls, product code LDD).
Submitted by Spacelabs, Inc. (Redmond, US). The FDA issued a Cleared decision on December 27, 1990, 384 days after receiving the submission on December 8, 1989.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.5300.
| 510(k) Number | K896903 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 08, 1989 |
| Decision Date | December 27, 1990 |
| Days to Decision | 384 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | LDD — Dc-defibrillator, Low-energy, (including Paddles) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.5300 |