DFA RESPIRATORY VIRUS SCREENING & ID KIT— 510(k) K022713

Substantially Equivalent

Diagnostic Hybrids, Inc.

FDA 510(k) clearance K022713 for DFA RESPIRATORY VIRUS SCREENING & ID KIT, Substantially Equivalent on 2002-12-18. Applicant: Diagnostic Hybrids, Inc..

Clearance details

Applicant: Diagnostic Hybrids, Inc.
Product code: Code GNW
Advisory panel: Microbiology
Date received: 2002-08-14
Decision date: 2002-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Athens, OH, US

Download summary PDF View on FDA.gov ↗

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