Submission Details
| 510(k) Number | K000958 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 24, 2000 |
| Decision Date | May 24, 2000 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
K000958 is an FDA 510(k) clearance for the ATAC PAK BUN REAGENT AND ATAC CALIBRATOR KITS, a Urease And Glutamic Dehydrogenase, Urea Nitrogen (Class II — Special Controls, product code CDQ), submitted by Elan Holdings, Inc. (Brea, US). The FDA issued a Cleared decision on May 24, 2000, 61 days after receiving the submission on March 24, 2000. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1770.
| 510(k) Number | K000958 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 24, 2000 |
| Decision Date | May 24, 2000 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CDQ — Urease And Glutamic Dehydrogenase, Urea Nitrogen |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 862.1770 |