K850177 is an FDA 510(k) clearance for the MATRIX DRI-IDEA (PLASTIC DISPOS. SURGICAL GOWN). This device is classified as a Gown, Surgical (Class II - Special Controls, product code FYA).
Submitted by Matrix Medica, Inc. (Minden, US). The FDA issued a Cleared decision on February 21, 1985, 35 days after receiving the submission on January 17, 1985.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 878.4040.
| 510(k) Number | K850177 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 17, 1985 |
| Decision Date | February 21, 1985 |
| Days to Decision | 35 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | — |
| Product Code | FYA — Gown, Surgical |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4040 |