RUBELLA MICROASSAY— 510(k) K864602

Substantially Equivalent

Diamedix Corp.

FDA 510(k) clearance K864602 for RUBELLA MICROASSAY, Substantially Equivalent on 1987-04-14. Applicant: Diamedix Corp.. Device class: 2.

Clearance details

Applicant: Diamedix Corp.
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1986-11-24
Decision date: 1987-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, 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.