K912772 is an FDA 510(k) clearance for the SUPERLOGGER. This device is classified as a Electrode, Ph, Stomach (Class I - General Controls, product code FFT).
Submitted by Sandhill Scientific, Inc. (Littleton, US). The FDA issued a Cleared decision on February 7, 1992, 228 days after receiving the submission on June 24, 1991.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1400.
| 510(k) Number | K912772 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 24, 1991 |
| Decision Date | February 07, 1992 |
| Days to Decision | 228 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FFT — Electrode, Ph, Stomach |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 876.1400 |