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FDA 510(k)

SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR

K-Number: K973914 · 1998-06-30

ApplicantSense Technology, Inc.
Decision Date1998-06-30
Product CodeLXM
DecisionSubstantially Equivalent

Device Summary

SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR is the device name listed in this FDA 510(k) record. The listed applicant is Sense Technology, Inc.. It received FDA 510(k) clearance on 1998-06-30 under 510(k) number K973914. The device is classified under product code LXM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR?

SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR is a medical device that received FDA 510(k) clearance on 1998-06-30. The listed applicant is Sense Technology, Inc.. The 510(k) number is K973914.

When did SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR receive FDA 510(k) clearance?

SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR received FDA 510(k) clearance on 1998-06-30, under 510(k) number K973914.

Who is the listed applicant for SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR?

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

What is the FDA product code for SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR?

The FDA product code for SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR is LXM.

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 Sense Technology, 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.

K940085FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01

Related Devices (Code: LXM)

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.

K234036SONIK MONARK 100Neuro Spinal Innovation, Inc.K192629SpinalyticsOptima Health Solutions International Corp.K172536Atlas Percussion Adjusting InstrumentSpinalight, Inc.K160278VSTAAR AdjusteRSpinal Acoustics, LLCK112606ACTIVATOR V-EActivator Methods International, Ltd.K082218MAX ADJUSTING INSTRUMENTManna Omni International, 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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