DeviceClearance

THYROID STIMULATING IMMUNOGLOBULIN REPORTER ASSAY— 510(k) K083391

Substantially Equivalent

Diagnostic Hybrids, Inc.

FDA 510(k) clearance K083391 for THYROID STIMULATING IMMUNOGLOBULIN REPORTER ASSAY, Substantially Equivalent on 2009-05-21. Applicant: Diagnostic Hybrids, Inc..

Clearance details

Applicant
Diagnostic Hybrids, Inc.
Product code
Code JZO
Advisory panel
Immunology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Athens, OH, US
Download summary PDFView on FDA.gov ↗

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