INSPIROMETER— 510(k) K833012

Substantially Equivalent

Kinetix

FDA 510(k) clearance K833012 for INSPIROMETER, Substantially Equivalent on 1983-11-08. Applicant: Kinetix. Device class: 2.

Clearance details

Applicant: Kinetix
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1983-09-06
Decision date: 1983-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, 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.