STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM— 510(k) K040369

Name: FDA 510(k) clearance K040369
Creator: U.S. Food and Drug Administration
Published: 2004-04-01

Substantially Equivalent

Stryker Instruments

FDA 510(k) clearance K040369 for STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM, Substantially Equivalent on 2004-04-01. Applicant: Stryker Instruments. Device class: 2.

Clearance details

Applicant: Stryker Instruments
Product code: Code DZJ
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2004-02-13
Decision date: 2004-04-01
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.