TENSMAX— 510(k) K811499

Substantially Equivalent

Anritsu America Co.

FDA 510(k) clearance K811499 for TENSMAX, Substantially Equivalent on 1981-08-20. Applicant: Anritsu America Co..

Clearance details

Applicant: Anritsu America Co.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 1981-05-27
Decision date: 1981-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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