MODEL 556 MONITOR— 510(k) K905856

Name: FDA 510(k) clearance K905856
Creator: U.S. Food and Drug Administration
Published: 1991-01-11

Substantially Equivalent

Ge Medical Systems Information Technologies

FDA 510(k) clearance K905856 for MODEL 556 MONITOR, Substantially Equivalent on 1991-01-11. Applicant: Ge Medical Systems Information Technologies. Device class: 1.

Clearance details

Applicant: Ge Medical Systems Information Technologies
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1990-10-15
Decision date: 1991-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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