TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER— 510(k) K862919

Name: FDA 510(k) clearance K862919
Creator: U.S. Food and Drug Administration
Published: 1986-11-07

Substantially Equivalent

Transpirator Technologics, Inc.

FDA 510(k) clearance K862919 for TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER, Substantially Equivalent on 1986-11-07. Applicant: Transpirator Technologics, Inc.. Device class: 1.

Clearance details

Applicant: Transpirator Technologics, Inc.
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1986-08-01
Decision date: 1986-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, NJ, US

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