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FDA 510(k)

RH-801, MODEL TRANSQ

K-Number: K925806 · 1994-07-14

ApplicantIomed, Inc.
Decision Date1994-07-14
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RH-801, MODEL TRANSQ is the device name listed in this FDA 510(k) record. The listed applicant is Iomed, Inc.. It received FDA 510(k) clearance on 1994-07-14 under 510(k) number K925806. 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 RH-801, MODEL TRANSQ?

RH-801, MODEL TRANSQ is a medical device that received FDA 510(k) clearance on 1994-07-14. The listed applicant is Iomed, Inc.. The 510(k) number is K925806.

When did RH-801, MODEL TRANSQ receive FDA 510(k) clearance?

RH-801, MODEL TRANSQ received FDA 510(k) clearance on 1994-07-14, under 510(k) number K925806.

Who is the listed applicant for RH-801, MODEL TRANSQ?

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 RH-801, MODEL TRANSQ?

The FDA product code for RH-801, MODEL TRANSQ 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 DEVICEK060236MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODEK033192RH-950K031115RH-900K001522TRANSQ3K001410PHORESOR MODEL PM2000

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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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