K870898 is an FDA 510(k) clearance for the ULTRA-LUX LIGHT SOURCE. This device is classified as a Light, Surgical, Endoscopic (Class II - Special Controls, product code FSW).
Submitted by Medline Industries, Inc. (Englewood, US). The FDA issued a Cleared decision on March 18, 1987, 13 days after receiving the submission on March 5, 1987.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4580.
| 510(k) Number | K870898 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 05, 1987 |
| Decision Date | March 18, 1987 |
| Days to Decision | 13 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | FSW — Light, Surgical, Endoscopic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4580 |