CARDIOSONIC ACOUSTIC AMPLIFIER— 510(k) K813510

Substantially Equivalent

Srs Co.

FDA 510(k) clearance K813510 for CARDIOSONIC ACOUSTIC AMPLIFIER, Substantially Equivalent on 1982-01-12. Applicant: Srs Co.. Device class: 1.

Clearance details

Applicant: Srs Co.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1981-12-15
Decision date: 1982-01-12
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.