K790928 is an FDA 510(k) clearance for the 3-WAY T 22MM MALE. This device is classified as a Tubing, Pressure And Accessories (Class I — General Controls, product code BYX).
Submitted by Mem Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 21, 1979, 6 days after receiving the submission on May 15, 1979.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5860.
| 510(k) Number | K790928 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 15, 1979 |
| Decision Date | May 21, 1979 |
| Days to Decision | 6 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | BYX — Tubing, Pressure And Accessories |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 868.5860 |