SPIROVIT, MODEL SP-250— 510(k) K984031

Substantially Equivalent

Schiller AG

FDA 510(k) clearance K984031 for SPIROVIT, MODEL SP-250, Substantially Equivalent on 1999-04-30. Applicant: Schiller AG. Device class: 2.

Clearance details

Applicant: Schiller AG
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1998-11-12
Decision date: 1999-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baar, CH

Download summary PDF View on FDA.gov ↗

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