K904330 is an FDA 510(k) clearance for the TURBO-RAST SPECIFIC IGE ASSAY. This device is classified as a System, Test, Radioallergosorbent (rast) Immunological (Class II - Special Controls, product code DHB).
Submitted by Ventrex Laboratories, Inc. (Portland, US). The FDA issued a Cleared decision on December 7, 1990, 78 days after receiving the submission on September 20, 1990.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5750.
| 510(k) Number | K904330 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 20, 1990 |
| Decision Date | December 07, 1990 |
| Days to Decision | 78 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | — |
| Product Code | DHB — System, Test, Radioallergosorbent (rast) Immunological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 866.5750 |