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FDA 510(k)

MD-2 IONTOPHORESIS UNIT

K-Number: K895365 · 1990-06-26

ApplicantR. A. Fischer Co. Corp.
Decision Date1990-06-26
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

MD-2 IONTOPHORESIS UNIT is the device name listed in this FDA 510(k) record. The listed applicant is R. A. Fischer Co. Corp.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K895365. 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 MD-2 IONTOPHORESIS UNIT?

MD-2 IONTOPHORESIS UNIT is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K895365.

When did MD-2 IONTOPHORESIS UNIT receive FDA 510(k) clearance?

MD-2 IONTOPHORESIS UNIT received FDA 510(k) clearance on 1990-06-26, under 510(k) number K895365.

Who is the listed applicant for MD-2 IONTOPHORESIS UNIT?

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

What is the FDA product code for MD-2 IONTOPHORESIS UNIT?

The FDA product code for MD-2 IONTOPHORESIS UNIT is EGJ.

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Other records listing R. A. Fischer Co. Corp. as applicant

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Related Devices (Code: EGJ)

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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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