STRYKER ADEL BASSINET— 510(k) K960012

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K960012 for STRYKER ADEL BASSINET, Substantially Equivalent on 1996-03-25. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code FMS
Device class: Class 2
Regulation: 21 CFR 880.5140
Advisory panel: General Hospital
Date received: 1996-01-02
Decision date: 1996-03-25
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.