STRYKER COMMAND2 OFFICE CONSOLE— 510(k) K953071

Name: FDA 510(k) clearance K953071
Creator: U.S. Food and Drug Administration
Published: 1995-08-08

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K953071 for STRYKER COMMAND2 OFFICE CONSOLE, Substantially Equivalent on 1995-08-08. Applicant: Stryker Instruments. Device class: 1.

Clearance details

Applicant: Stryker Instruments
Product code: Code JEA
Device class: Class 1
Regulation: 21 CFR 878.4960
Advisory panel: General, Plastic Surgery
Date received: 1995-06-30
Decision date: 1995-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.