SPIROVIT SP-2, PNEUMOCHECK II— 510(k) K992823

Substantially Equivalent

Schiller AG

FDA 510(k) clearance K992823 for SPIROVIT SP-2, PNEUMOCHECK II, Substantially Equivalent on 2000-05-12. 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: 1999-08-23
Decision date: 2000-05-12
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.