EBV/EA-CHECK TM TEST KIT— 510(k) K903612

Substantially Equivalent

Diagnostic Technology, Inc.

FDA 510(k) clearance K903612 for EBV/EA-CHECK TM TEST KIT, Substantially Equivalent on 1990-10-16. Applicant: Diagnostic Technology, Inc..

Clearance details

Applicant: Diagnostic Technology, Inc.
Product code: Code LSE
Advisory panel: Microbiology
Date received: 1990-08-09
Decision date: 1990-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

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