CRYSTAL TRACE PIEZO RESPIRATORY EFFORT SENSOR— 510(k) K923402

Name: FDA 510(k) clearance K923402
Creator: U.S. Food and Drug Administration
Published: 1992-12-30

Substantially Equivalent

Pro-Tech, Inc.

FDA 510(k) clearance K923402 for CRYSTAL TRACE PIEZO RESPIRATORY EFFORT SENSOR, Substantially Equivalent on 1992-12-30. Applicant: Pro-Tech, Inc.. Device class: 2.

Clearance details

Applicant: Pro-Tech, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1992-07-10
Decision date: 1992-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodinville, WA, US

Download summary PDF View on FDA.gov ↗

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