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FDA 510(k)

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE

K-Number: K894549 · 1990-02-09

ApplicantHenley Intl.
Decision Date1990-02-09
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Henley Intl.. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K894549. 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 DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE?

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Henley Intl.. The 510(k) number is K894549.

When did DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE receive FDA 510(k) clearance?

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE received FDA 510(k) clearance on 1990-02-09, under 510(k) number K894549.

Who is the listed applicant for DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE?

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

What is the FDA product code for DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE?

The FDA product code for DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE is EGJ.

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Other records listing Henley Intl. 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.

K943449NEUROLOGICAL DIAGNOSTIC DEVICESK926279UPPER BODY EXERCISERK926278STAIR CLIMBERK926287EXERCISE BICYCLEK926314HYDRA FITNESS MODEL 311 TOTAL POWERK926313COMPUTERIZED TESTING AND EXERCISE SYSTEMS

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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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