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FDA 510(k)

NOROTRACK 360 INCLINOMETER

K-Number: K920690 · 1992-05-20

ApplicantNoromed, Inc.
Decision Date1992-05-20
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NOROTRACK 360 INCLINOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Noromed, Inc.. It received FDA 510(k) clearance on 1992-05-20 under 510(k) number K920690. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOROTRACK 360 INCLINOMETER?

NOROTRACK 360 INCLINOMETER is a medical device that received FDA 510(k) clearance on 1992-05-20. The listed applicant is Noromed, Inc.. The 510(k) number is K920690.

When did NOROTRACK 360 INCLINOMETER receive FDA 510(k) clearance?

NOROTRACK 360 INCLINOMETER received FDA 510(k) clearance on 1992-05-20, under 510(k) number K920690.

Who is the listed applicant for NOROTRACK 360 INCLINOMETER?

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

What is the FDA product code for NOROTRACK 360 INCLINOMETER?

The FDA product code for NOROTRACK 360 INCLINOMETER is KQX.

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 Noromed, 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.

K922838NORODYN 2000 ELECTROMYOGRAPH

Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, 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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