OMNI STIK— 510(k) K781616

Substantially Equivalent

Unitron Corp.

FDA 510(k) clearance K781616 for OMNI STIK, Substantially Equivalent on 1978-12-08. Applicant: Unitron Corp.. Device class: 1.

Clearance details

Applicant: Unitron Corp.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1978-09-20
Decision date: 1978-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.