FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01— 510(k) K992256

Name: FDA 510(k) clearance K992256
Creator: U.S. Food and Drug Administration
Published: 2000-01-11

Substantially Equivalent

Intercontinental New Technologies, Inc.

FDA 510(k) clearance K992256 for FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01, Substantially Equivalent on 2000-01-11. Applicant: Intercontinental New Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Intercontinental New Technologies, Inc.
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1999-07-06
Decision date: 2000-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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