QUANTA LITE(TM) ACA— 510(k) K911680

Substantially Equivalent

Inova Diagnostics, Inc.

FDA 510(k) clearance K911680 for QUANTA LITE(TM) ACA, Substantially Equivalent on 1991-11-19. Applicant: Inova Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Inova Diagnostics, Inc.
Product code: Code MID
Device class: Class 2
Regulation: 21 CFR 866.5660
Advisory panel: Immunology
Date received: 1991-04-15
Decision date: 1991-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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