VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K— 510(k) K972922

Name: FDA 510(k) clearance K972922
Creator: U.S. Food and Drug Administration
Published: 1997-10-08

Substantially Equivalent

Interview Medical Technology Corp.

FDA 510(k) clearance K972922 for VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K, Substantially Equivalent on 1997-10-08. Applicant: Interview Medical Technology Corp.. Device class: 1.

Clearance details

Applicant: Interview Medical Technology Corp.
Product code: Code EMX
Device class: Class 1
Regulation: 21 CFR 874.4100
Advisory panel: Ear, Nose, Throat
Date received: 1997-08-08
Decision date: 1997-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: El Dorado Hills, CA, US

Download summary PDF View on FDA.gov ↗

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