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FDA 510(k)

IMPERIUM

K-Number: K953905 · 1995-11-21

ApplicantTeledyne Brown Engineering
Decision Date1995-11-21
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IMPERIUM is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Brown Engineering. It received FDA 510(k) clearance on 1995-11-21 under 510(k) number K953905. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPERIUM?

IMPERIUM is a medical device that received FDA 510(k) clearance on 1995-11-21. The listed applicant is Teledyne Brown Engineering. The 510(k) number is K953905.

When did IMPERIUM receive FDA 510(k) clearance?

IMPERIUM received FDA 510(k) clearance on 1995-11-21, under 510(k) number K953905.

Who is the listed applicant for IMPERIUM?

The FDA 510(k) record lists Teledyne Brown Engineering as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPERIUM?

The FDA product code for IMPERIUM is IQA.

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 Teledyne Brown Engineering 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.

K963177TED 191

Related Devices (Code: IQA)

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.

K961306DELTATALKER WITH INFRAREDPrentke Romich Co.K953937LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEMApt Technology, Inc.K943244DEUCEApt Technology, Inc.K944585SCANNING DIRECTORPrentke Romich Co.K944345BEDSIDE BUTLERTrac Medical, Inc.K940223LEARN MODE WATERPROOF PENDANT PANIC BUTTONInteractive Technologies, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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