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FDA 510(k)

NEUROMETER

K-Number: K853608 · 1986-06-12

ApplicantNeurotron, Inc.
Decision Date1986-06-12
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Neurotron, Inc.. It received FDA 510(k) clearance on 1986-06-12 under 510(k) number K853608. The device is classified under product code LLN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMETER?

NEUROMETER is a medical device that received FDA 510(k) clearance on 1986-06-12. The listed applicant is Neurotron, Inc.. The 510(k) number is K853608.

When did NEUROMETER receive FDA 510(k) clearance?

NEUROMETER received FDA 510(k) clearance on 1986-06-12, under 510(k) number K853608.

Who is the listed applicant for NEUROMETER?

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

What is the FDA product code for NEUROMETER?

The FDA product code for NEUROMETER is LLN.

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 Neurotron, 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.

K843924DIGITAL ELECTRONEUROMETER S-100

Related Devices (Code: LLN)

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.

K072882PAIN VISION, MODEL PS-2100Osachi Co., Ltd.K030829VPT METERXilas Medical, Inc.K010981GSA GENITO SENSORY ANALYZERMedoc Ltd. Advanced Medical SystemsK964622MEDI-DX 7000Neuro-Diagnostic Assoc.K964815AP-4000, AIR PULSE SENSORY STIMULATORPentax Precision Instrument Corp.K970180VSA 3000 VIBRATORYN SENSORY ANALYZEREare Consulting Service

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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