VASOPULSE(TM)/MODEL 5000— 510(k) K863803

Substantially Equivalent

Sonicaid, Inc.

FDA 510(k) clearance K863803 for VASOPULSE(TM)/MODEL 5000, Substantially Equivalent on 1987-05-06. Applicant: Sonicaid, Inc.. Device class: 2.

Clearance details

Applicant: Sonicaid, Inc.
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1986-09-29
Decision date: 1987-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fredericksburg, VA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Sonicaid, Inc.

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