DISPIRO— 510(k) K791177

Substantially Equivalent

Utah Medical Products, Inc.

FDA 510(k) clearance K791177 for DISPIRO, Substantially Equivalent on 1979-08-10. Applicant: Utah Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Utah Medical Products, Inc.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1979-06-25
Decision date: 1979-08-10
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.