AMPLITONE-3— 510(k) K812676

Substantially Equivalent

Progressive Technology, Inc.

FDA 510(k) clearance K812676 for AMPLITONE-3, Substantially Equivalent on 1981-10-13. Applicant: Progressive Technology, Inc..

Clearance details

Applicant: Progressive Technology, Inc.
Product code: Code LDE
Advisory panel: Cardiovascular
Date received: 1981-09-22
Decision date: 1981-10-13
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.