SCANLISA HUMAN CRP ELISA KIT— 510(k) K894573

Substantially Equivalent

Immuntech A/S

FDA 510(k) clearance K894573 for SCANLISA HUMAN CRP ELISA KIT, Substantially Equivalent on 1989-08-10. Applicant: Immuntech A/S. Device class: 2.

Clearance details

Applicant: Immuntech A/S
Product code: Code DCK
Device class: Class 2
Regulation: 21 CFR 866.5270
Advisory panel: Immunology
Date received: 1989-07-21
Decision date: 1989-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denmark, DK

Download summary PDF View on FDA.gov ↗

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