
Bayer Corp.
Free shipping on orders over $99 · 30-day returns
PROGESTERONE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-BITRO DIAGNOSTIC SYSTEM is an FDA 510(k)-cleared medical device (K952075) manufactured by Bayer Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 12, 1995. Regulation: 8.