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NanoKnife Generator (H78720300301US0) +3 more models

FDA 510(k)

Class II (US FDA 510(k))

510(k) K242687

by Angiodynamics, Inc.

Identifiers

510(k) Number
K242687 FDA 510(k)
FDA Product Code
OAB FDA 510(k)
Models / Variants
NanoKnife Generator (H78720300301US0) FDA 510(k)
NanoKnife Single Electrode Activation Probe, 15 cm (H787204001090) FDA 510(k)
NanoKnife Single Electrode Activation Probe, 25 cm (H787204001100) FDA 510(k)
NanoKnife Single Electrode Probe Spacer (H787204003010) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4400 FDA 510(k)
Regulation Number
878.4400 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

NanoKnife Generator (H78720300301US0) +3 more models by Angiodynamics, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 4 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Angiodynamics, Inc.

Sources (1)

  • FDA 510(k) K242687 24 fields · synced Jun 18, 2026