ADEL 5000— 510(k) K950889

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K950889 for ADEL 5000, Substantially Equivalent on 1995-10-16. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code HDD
Device class: Class 2
Regulation: 21 CFR 884.4900
Advisory panel: Obstetrics/Gynecology
Date received: 1995-02-28
Decision date: 1995-10-16
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.