QUANTA LITE(TM) IGA ACA— 510(k) K922351

Substantially Equivalent

Inova Diagnostics, Inc.

FDA 510(k) clearance K922351 for QUANTA LITE(TM) IGA ACA, Substantially Equivalent on 1992-09-29. Applicant: Inova Diagnostics, Inc..

Clearance details

Applicant: Inova Diagnostics, Inc.
Product code: Code MID
Advisory panel: Immunology
Date received: 1992-05-19
Decision date: 1992-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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