RHINOMANOMETER A440 DIGITAL— 510(k) K844230

Name: FDA 510(k) clearance K844230
Creator: U.S. Food and Drug Administration
Published: 1984-11-27

Substantially Equivalent

Center Laboratories, Inc.

FDA 510(k) clearance K844230 for RHINOMANOMETER A440 DIGITAL, Substantially Equivalent on 1984-11-27. Applicant: Center Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Center Laboratories, Inc.
Product code: Code BXQ
Device class: Class 2
Regulation: 21 CFR 868.1800
Advisory panel: Anesthesiology
Date received: 1984-11-01
Decision date: 1984-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Washington, NY, US

Download summary PDF View on FDA.gov ↗

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