NOZOVENT, NASAL DILATOR— 510(k) K904290

Name: FDA 510(k) clearance K904290
Creator: U.S. Food and Drug Administration
Published: 1991-08-20

Substantially Equivalent

Wpm Intl AB Intl Trade & Managemet Consulting

FDA 510(k) clearance K904290 for NOZOVENT, NASAL DILATOR, Substantially Equivalent on 1991-08-20. Applicant: Wpm Intl AB Intl Trade & Managemet Consulting. Device class: 1.

Clearance details

Applicant: Wpm Intl AB Intl Trade & Managemet Consulting
Product code: Code LWF
Device class: Class 1
Regulation: 21 CFR 874.3900
Advisory panel: Ear, Nose, Throat
Date received: 1990-09-17
Decision date: 1991-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sweden, SE

Download summary PDF View on FDA.gov ↗

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