K781921 is an FDA 510(k) clearance for the BILIRUBIN, DINGLE VALVE DPD. This device is classified as a Diazo Colorimetry, Bilirubin (Class II - Special Controls, product code CIG).
Submitted by Boehringer Mannheim Corp. (Mchenry, US). The FDA issued a Cleared decision on January 3, 1979, 51 days after receiving the submission on November 13, 1978.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1110.
| 510(k) Number | K781921 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 13, 1978 |
| Decision Date | January 03, 1979 |
| Days to Decision | 51 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CIG — Diazo Colorimetry, Bilirubin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1110 |