SONICAID MODEL D206E AIR EMBOLI-DETECT— 510(k) K833227

Name: FDA 510(k) clearance K833227
Creator: U.S. Food and Drug Administration
Published: 1983-10-27

Substantially Equivalent

Sonicaid, Inc.

FDA 510(k) clearance K833227 for SONICAID MODEL D206E AIR EMBOLI-DETECT, Substantially Equivalent on 1983-10-27. Applicant: Sonicaid, Inc.. Device class: 1.

Clearance details

Applicant: Sonicaid, Inc.
Product code: Code LBA
Device class: Class 1
Regulation: 21 CFR 862.3280
Advisory panel: Clinical Toxicology
Date received: 1983-08-16
Decision date: 1983-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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