MODEL 9300 ELECTROCARDIOVALIDATOR— 510(k) K801830

Name: FDA 510(k) clearance K801830
Creator: U.S. Food and Drug Administration
Published: 1980-08-27

Substantially Equivalent

Del Mar Avionics

FDA 510(k) clearance K801830 for MODEL 9300 ELECTROCARDIOVALIDATOR, Substantially Equivalent on 1980-08-27. Applicant: Del Mar Avionics. Device class: 1.

Clearance details

Applicant: Del Mar Avionics
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1980-08-01
Decision date: 1980-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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