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FDA 510(k)

MINIPHYSIONIZER 2.0 AND ELECTRODES

K-Number: K022950 · 2003-04-18

ApplicantPhysion, Inc.
Decision Date2003-04-18
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MINIPHYSIONIZER 2.0 AND ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Physion, Inc.. It received FDA 510(k) clearance on 2003-04-18 under 510(k) number K022950. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIPHYSIONIZER 2.0 AND ELECTRODES?

MINIPHYSIONIZER 2.0 AND ELECTRODES is a medical device that received FDA 510(k) clearance on 2003-04-18. The listed applicant is Physion, Inc.. The 510(k) number is K022950.

When did MINIPHYSIONIZER 2.0 AND ELECTRODES receive FDA 510(k) clearance?

MINIPHYSIONIZER 2.0 AND ELECTRODES received FDA 510(k) clearance on 2003-04-18, under 510(k) number K022950.

Who is the listed applicant for MINIPHYSIONIZER 2.0 AND ELECTRODES?

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

What is the FDA product code for MINIPHYSIONIZER 2.0 AND ELECTRODES?

The FDA product code for MINIPHYSIONIZER 2.0 AND ELECTRODES is EGJ.

Related Clinical Trials

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.

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Other records listing Physion, Inc. 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.

K043383N-DO ENDOINJECTOR NEEDLE, MODEL PH00961109 AND PH00961110

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

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

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