K161082 is an FDA 510(k) clearance for the IDS-iSYS 17-OH Progesterone Control Set, IDS-iSYS 17-OH Progesterone Calibration Verifiers. This device is classified as a Single (specified) Analyte Controls (assayed And Unassayed) (Class I - General Controls, product code JJX).
Submitted by Immunodiagnostic Systems , Ltd. (Boldon, GB). The FDA issued a Cleared decision on May 17, 2016, 29 days after receiving the submission on April 18, 2016.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1660.