RESPI-PAK RT-PAK— 510(k) K910452

Substantially Equivalent

Cns, Inc.

FDA 510(k) clearance K910452 for RESPI-PAK RT-PAK, Substantially Equivalent on 1991-04-16. Applicant: Cns, Inc.. Device class: 2.

Clearance details

Applicant: Cns, Inc.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1991-02-01
Decision date: 1991-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, 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.