DATASON DB ULTRASOUND IMAGING SYSTEM— 510(k) K810305

Name: FDA 510(k) clearance K810305
Creator: U.S. Food and Drug Administration
Published: 1981-03-13

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K810305 for DATASON DB ULTRASOUND IMAGING SYSTEM, Substantially Equivalent on 1981-03-13. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code HEM
Device class: Class 2
Regulation: 21 CFR 884.2225
Advisory panel: Obstetrics/Gynecology
Date received: 1981-02-05
Decision date: 1981-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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