VIROTHERM HUMIDIFIER— 510(k) K915603

Substantially Equivalent

Virotherm Laboratory

FDA 510(k) clearance K915603 for VIROTHERM HUMIDIFIER, Substantially Equivalent on 1992-10-22. Applicant: Virotherm Laboratory. Device class: 1.

Clearance details

Applicant: Virotherm Laboratory
Product code: Code KFZ
Device class: Class 1
Regulation: 21 CFR 868.5460
Advisory panel: Anesthesiology
Date received: 1991-12-16
Decision date: 1992-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saratoga, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KFZ

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K871189 — SUNBEAM DURA-VAP WARM STEAM VAPORIZER MODEL 13801987-05-08
K862919 — TRANSPIRATOR(TM) MT-1000 PERSONAL HUMIDIFIER1986-11-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.