THYROGLOBULIN EIA TEST KIT— 510(k) K951362

Substantially Equivalent

Immunoprobe, Inc.

FDA 510(k) clearance K951362 for THYROGLOBULIN EIA TEST KIT, Substantially Equivalent on 1995-11-20. Applicant: Immunoprobe, Inc.. Device class: 2.

Clearance details

Applicant: Immunoprobe, Inc.
Product code: Code JNL
Device class: Class 2
Regulation: 21 CFR 866.5870
Advisory panel: Immunology
Date received: 1995-03-24
Decision date: 1995-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, D.C., DC, US

Download summary PDF View on FDA.gov ↗

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