K861863 is an FDA 510(k) clearance for the MODIFIED PROTECTIVE GARMENT. This device is classified as a Garment, Protective, For Incontinence (Class I - General Controls, product code EYQ).
Submitted by Procter & Gamble Mfg. Co. (Cincinnati, US). The FDA issued a Cleared decision on August 11, 1986, 88 days after receiving the submission on May 15, 1986.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5920.
| 510(k) Number | K861863 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 15, 1986 |
| Decision Date | August 11, 1986 |
| Days to Decision | 88 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | — |
| Product Code | EYQ — Garment, Protective, For Incontinence |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 876.5920 |