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TipVision Videoscope System (TipVision VideoScope 0°/30° +1 more model

FDA 510(k)

Class II (US FDA 510(k))

510(k) K201617

by Schoelly Fiberoptic GmbH

Identifiers

510(k) Number
K201617 FDA 510(k)
FDA Product Code
HET FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 884.1720 FDA 510(k)
Regulation Number
884.1720 FDA 510(k)
Advisory Committee
Obstetrics/Gynecology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

TipVision Videoscope System (TipVision VideoScope 0°/30° +1 more model by Schoelly Fiberoptic GmbH — Class II — FDA_510K — listed in FDA 510(k) — 2 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Sources (1)

  • FDA 510(k) K201617 24 fields · synced Jun 18, 2026