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FDA 510(k)

DYNATRON IBOX IONTOPHORESIS DEVICE

K-Number: K043047 · 2005-01-07

ApplicantDynatronics Corp.
Decision Date2005-01-07
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

DYNATRON IBOX IONTOPHORESIS DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatronics Corp.. It received FDA 510(k) clearance on 2005-01-07 under 510(k) number K043047. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DYNATRON IBOX IONTOPHORESIS DEVICE?

DYNATRON IBOX IONTOPHORESIS DEVICE is a medical device that received FDA 510(k) clearance on 2005-01-07. The listed applicant is Dynatronics Corp.. The 510(k) number is K043047.

When did DYNATRON IBOX IONTOPHORESIS DEVICE receive FDA 510(k) clearance?

DYNATRON IBOX IONTOPHORESIS DEVICE received FDA 510(k) clearance on 2005-01-07, under 510(k) number K043047.

Who is the listed applicant for DYNATRON IBOX IONTOPHORESIS DEVICE?

The FDA 510(k) record lists Dynatronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNATRON IBOX IONTOPHORESIS DEVICE?

The FDA product code for DYNATRON IBOX IONTOPHORESIS DEVICE is EGJ.

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Other records listing Dynatronics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113250DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBEK060814DYNATRON ION IONTOPHORESIS ELECTRODEK051680DYNATRON DX2 TRACTION UNITK051261DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBEK040729SOLARIS D890 THERAPY PROBEK031329DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY)

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Related Devices (Code: EGJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242041STOPWET iontophoresis apparatus (SW01)Taiwan Medical Electronics Co., Ltd.K241267Hidroxa SE30Hidroxa Medical ABK232020Iontophoresis ElectrodesTop-Rank Health Care Co., Ltd.K192749DermadryDermadry Laboratories, Inc.K191436SaalioSaalmann Medical GmbH & Co. KGK170835Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITEHightech Development

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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