RDI LDL PRECIPITATION REAGENT— 510(k) K964063

Substantially Equivalent

Reference Diagnostics, Inc.

FDA 510(k) clearance K964063 for RDI LDL PRECIPITATION REAGENT, Substantially Equivalent on 1996-11-20. Applicant: Reference Diagnostics, Inc..

Clearance details

Applicant: Reference Diagnostics, Inc.
Product code: Code MRR
Advisory panel: Clinical Chemistry
Date received: 1996-10-10
Decision date: 1996-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bedford, MA, US

Download summary PDF View on FDA.gov ↗

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