K950087 is an FDA 510(k) clearance for the LOT 440, a Electrode, Ph, Stomach (Class I — General Controls, product code FFT), submitted by Medical Instruments Corporation Mic AG (Solothurn, CH). The FDA issued a Cleared decision on February 6, 1996, 392 days after receiving the submission on January 10, 1995. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1400.
| 510(k) Number | K950087 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 10, 1995 |
| Decision Date | February 06, 1996 |
| Days to Decision | 392 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | FFT — Electrode, Ph, Stomach |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 876.1400 |