K896852 is an FDA 510(k) clearance for the VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY. 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 18, 1989, 13 days after receiving the submission on December 5, 1989.
This device falls under the Immunology FDA review panel. Regulated under 21 CFR 866.5750.
| 510(k) Number | K896852 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 05, 1989 |
| Decision Date | December 18, 1989 |
| Days to Decision | 13 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 |