ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE— 510(k) K900560

Name: FDA 510(k) clearance K900560
Creator: U.S. Food and Drug Administration
Published: 1990-12-03

Substantially Equivalent

Acuson Corp.

FDA 510(k) clearance K900560 for ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE, Substantially Equivalent on 1990-12-03. Applicant: Acuson Corp.. Device class: 1.

Clearance details

Applicant: Acuson Corp.
Product code: Code DQC
Device class: Class 1
Regulation: 21 CFR 870.2390
Advisory panel: Cardiovascular
Date received: 1990-02-07
Decision date: 1990-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, 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.