SSD-725 ULTRASOUND SECTOR SCANNER— 510(k) K870607

Name: FDA 510(k) clearance K870607
Creator: U.S. Food and Drug Administration
Published: 1987-08-10

Substantially Equivalent

Ge Medical Systems Information Technologies

FDA 510(k) clearance K870607 for SSD-725 ULTRASOUND SECTOR SCANNER, Substantially Equivalent on 1987-08-10. Applicant: Ge Medical Systems Information Technologies. Device class: 2.

Clearance details

Applicant: Ge Medical Systems Information Technologies
Product code: Code JOP
Device class: Class 2
Regulation: 21 CFR 870.2880
Advisory panel: Cardiovascular
Date received: 1987-02-11
Decision date: 1987-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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