PRESTO DIAGNOSTIC SPIROMETER— 510(k) K894997

Name: FDA 510(k) clearance K894997
Creator: U.S. Food and Drug Administration
Published: 1989-10-30

Substantially Equivalent

Tamarac Systems Corp.

FDA 510(k) clearance K894997 for PRESTO DIAGNOSTIC SPIROMETER, Substantially Equivalent on 1989-10-30. Applicant: Tamarac Systems Corp.. Device class: 2.

Clearance details

Applicant: Tamarac Systems Corp.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 1989-08-08
Decision date: 1989-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

Download summary PDF View on FDA.gov ↗

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