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FDA 510(k)

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE

K-Number: K060236 · 2006-03-31

ApplicantIomed, Inc.
Decision Date2006-03-31
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Iomed, Inc.. It received FDA 510(k) clearance on 2006-03-31 under 510(k) number K060236. 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 MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE?

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE is a medical device that received FDA 510(k) clearance on 2006-03-31. The listed applicant is Iomed, Inc.. The 510(k) number is K060236.

When did MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE receive FDA 510(k) clearance?

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE received FDA 510(k) clearance on 2006-03-31, under 510(k) number K060236.

Who is the listed applicant for MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE?

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

What is the FDA product code for MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE?

The FDA product code for MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE is EGJ.

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Other records listing Iomed, 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.

K063465CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICEK033192RH-950K031115RH-900K001522TRANSQ3K001410PHORESOR MODEL PM2000K982668PHORESOR II,MODEL PM900

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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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