Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TRANSQ 2

K-Number: K914264 · 1991-12-20

ApplicantIomed, Inc.
Decision Date1991-12-20
Product CodeEGJ
Advisory CommitteePM
DecisionUnknown

Device Summary

TRANSQ 2 is the device name listed in this FDA 510(k) record. The listed applicant is Iomed, Inc.. It received FDA 510(k) clearance on 1991-12-20 under 510(k) number K914264. 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 TRANSQ 2?

TRANSQ 2 is a medical device that received FDA 510(k) clearance on 1991-12-20. The listed applicant is Iomed, Inc.. The 510(k) number is K914264.

When did TRANSQ 2 receive FDA 510(k) clearance?

TRANSQ 2 received FDA 510(k) clearance on 1991-12-20, under 510(k) number K914264.

Who is the listed applicant for TRANSQ 2?

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 TRANSQ 2?

The FDA product code for TRANSQ 2 is EGJ.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 17 devices →

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.

↑