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FDA 510(k)

VSA 3000 VIBRATORYN SENSORY ANALYZER

K-Number: K970180 · 1997-04-25

ApplicantEare Consulting Service
Decision Date1997-04-25
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VSA 3000 VIBRATORYN SENSORY ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Eare Consulting Service. It received FDA 510(k) clearance on 1997-04-25 under 510(k) number K970180. 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 VSA 3000 VIBRATORYN SENSORY ANALYZER?

VSA 3000 VIBRATORYN SENSORY ANALYZER is a medical device that received FDA 510(k) clearance on 1997-04-25. The listed applicant is Eare Consulting Service. The 510(k) number is K970180.

When did VSA 3000 VIBRATORYN SENSORY ANALYZER receive FDA 510(k) clearance?

VSA 3000 VIBRATORYN SENSORY ANALYZER received FDA 510(k) clearance on 1997-04-25, under 510(k) number K970180.

Who is the listed applicant for VSA 3000 VIBRATORYN SENSORY ANALYZER?

The FDA 510(k) record lists Eare Consulting Service as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VSA 3000 VIBRATORYN SENSORY ANALYZER?

The FDA product code for VSA 3000 VIBRATORYN SENSORY ANALYZER 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 Eare Consulting Service 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.

K950592ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURESK944428LITE-BLADEK934981DENTAL DRILL

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.K934368NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001Nk Biotechnical Engineering Co.

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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