Submission Details
| 510(k) Number | K122197 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 24, 2012 |
| Decision Date | August 28, 2013 |
| Days to Decision | 400 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Summary PDF |
K122197 is an FDA 510(k) clearance for the AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES, a System, Test, Radioallergosorbent (rast) Immunological (Class II — Special Controls, product code DHB), submitted by Phadia US, Inc. (Portae, US). The FDA issued a Cleared decision on August 28, 2013, 400 days after receiving the submission on July 24, 2012. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5750.
| 510(k) Number | K122197 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 24, 2012 |
| Decision Date | August 28, 2013 |
| Days to Decision | 400 days |
| Submission Type | Traditional |
| Review Panel | Immunology (IM) |
| Summary | Summary PDF |
| Product Code | DHB — System, Test, Radioallergosorbent (rast) Immunological |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 866.5750 |