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FDA 510(k)

TRANSQ3

K-Number: K001522 · 2000-10-18

ApplicantIomed, Inc.
Decision Date2000-10-18
Product CodeKTB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRANSQ3 is the device name listed in this FDA 510(k) record. The listed applicant is Iomed, Inc.. It received FDA 510(k) clearance on 2000-10-18 under 510(k) number K001522. The device is classified under product code KTB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSQ3?

TRANSQ3 is a medical device that received FDA 510(k) clearance on 2000-10-18. The listed applicant is Iomed, Inc.. The 510(k) number is K001522.

When did TRANSQ3 receive FDA 510(k) clearance?

TRANSQ3 received FDA 510(k) clearance on 2000-10-18, under 510(k) number K001522.

Who is the listed applicant for TRANSQ3?

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 TRANSQ3?

The FDA product code for TRANSQ3 is KTB.

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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 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-900K001410PHORESOR MODEL PM2000K982668PHORESOR II,MODEL PM900

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Related Devices (Code: KTB)

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.

K180627Macroduct Advanced Model 3710Elitechgroup, Inc.K033192RH-950Iomed, Inc.K031551NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D)Vyteris, Inc.K031115RH-900Iomed, Inc.K010031NANODUCT NEONATAL SWEAT ANALYSIS SYSTEMWescor, Inc.K001410PHORESOR MODEL PM2000Iomed, Inc.

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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