KINETIX MOUTHPIECE— 510(k) K833420

Substantially Equivalent

Kinetix

FDA 510(k) clearance K833420 for KINETIX MOUTHPIECE, Substantially Equivalent on 1984-01-10. Applicant: Kinetix. Device class: 1.

Clearance details

Applicant: Kinetix
Product code: Code BYP
Device class: Class 1
Regulation: 21 CFR 868.5620
Advisory panel: Anesthesiology
Date received: 1983-10-03
Decision date: 1984-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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