VIALON SURGEON'S GLOVES— 510(k) K802027

Substantially Equivalent

Rivefain Corp.

FDA 510(k) clearance K802027 for VIALON SURGEON'S GLOVES, Substantially Equivalent on 1980-10-10. Applicant: Rivefain Corp.. Device class: 1.

Clearance details

Applicant
Rivefain Corp.
Product code
Code KGO
Device class
Class 1
Regulation
21 CFR 878.4460
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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