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# FDA Revokes Emergency Use OK for Zika Test
- URL: https://www.fdaweb.com/fda-revokes-emergency-use-ok-for-zika-test/
- Published: 2019-08-07T12:00:00.000Z
- Updated: 2026-09-15T01:42:31.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5144707

*Federal Register* notice: FDA has revoked an Emergency Use Authorization issued to InBios International for the ZIKV Detect 2.0 IgM Capture ELISA based on the company gaining *de novo* marketing clearance 5/23 for the Class 2 device under the generic name “Zika virus serological reagents.” To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2019-08-07/pdf/2019-16881.pdf?ref=fdaweb.com).