SPIROTECH 300— 510(k) K823771

Substantially Equivalent

Spirotech, Inc.

FDA 510(k) clearance K823771 for SPIROTECH 300, Substantially Equivalent on 1983-01-28. Applicant: Spirotech, Inc.. Device class: 2.

Clearance details

Applicant: Spirotech, Inc.
Product code: Code BTY
Device class: Class 2
Regulation: 21 CFR 868.1890
Advisory panel: Anesthesiology
Date received: 1982-12-14
Decision date: 1983-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Spirotech, Inc.

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