K791922 is an FDA 510(k) clearance for the HARLECO BRAND CLINICARD LIPASE TEST SET. This device is classified as a Olive Oil Emulsion (turbidimetric), Lipase (Class I - General Controls, product code CET).
Submitted by Dade, Baxter Travenol Diagnostics, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 27, 1979, 62 days after receiving the submission on September 26, 1979.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1465.
| 510(k) Number | K791922 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 26, 1979 |
| Decision Date | November 27, 1979 |
| Days to Decision | 62 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CET — Olive Oil Emulsion (turbidimetric), Lipase |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1465 |