TRANSESOPHAGEAL ECHO TRANSDUCER— 510(k) K883889

Name: FDA 510(k) clearance K883889
Creator: U.S. Food and Drug Administration
Published: 1988-11-29

Substantially Equivalent

General Electric Co.

FDA 510(k) clearance K883889 for TRANSESOPHAGEAL ECHO TRANSDUCER, Substantially Equivalent on 1988-11-29. Applicant: General Electric Co.. Device class: 2.

Clearance details

Applicant: General Electric Co.
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1988-09-14
Decision date: 1988-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

Download summary PDF View on FDA.gov ↗

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