MODIFICATION TO TRUZONE PEAK FLOW METER— 510(k) K991212

Name: FDA 510(k) clearance K991212
Creator: U.S. Food and Drug Administration
Published: 1999-07-01

Substantially Equivalent

Monaghan Medical Corp.

FDA 510(k) clearance K991212 for MODIFICATION TO TRUZONE PEAK FLOW METER, Substantially Equivalent on 1999-07-01. Applicant: Monaghan Medical Corp.. Device class: 2.

Clearance details

Applicant: Monaghan Medical Corp.
Product code: Code BZH
Device class: Class 2
Regulation: 21 CFR 868.1860
Advisory panel: Anesthesiology
Date received: 1999-04-09
Decision date: 1999-07-01
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Plattsburgh, NY, US

Download summary PDF View on FDA.gov ↗

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