PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH— 510(k) K873431

Substantially Equivalent

Serono Diagnostics, Inc.

FDA 510(k) clearance K873431 for PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH, Substantially Equivalent on 1987-10-20. Applicant: Serono Diagnostics, Inc..

Clearance details

Applicant: Serono Diagnostics, Inc.
Product code: Code JLS
Advisory panel: Clinical Chemistry
Date received: 1987-08-26
Decision date: 1987-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwell, MA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.