K770169 is an FDA 510(k) clearance for the BEESON AUTOMADDAK FEEDER. This device is classified as a Utensil, Eating (Class I - General Controls, product code ILC).
Submitted by Techhnilab Instruments, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 28, 1977, 3 days after receiving the submission on January 25, 1977.
This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.5050.
| 510(k) Number | K770169 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 25, 1977 |
| Decision Date | January 28, 1977 |
| Days to Decision | 3 days |
| Submission Type | Traditional |
| Review Panel | Physical Medicine (PM) |
| Summary | — |
| Product Code | ILC — Utensil, Eating |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 890.5050 |