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FDA 510(k)

CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4

K-Number: K910624 · 1992-01-17

ApplicantWr Medical Electronics Co.
Decision Date1992-01-17
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 is the device name listed in this FDA 510(k) record. The listed applicant is Wr Medical Electronics Co.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K910624. 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 CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4?

CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Wr Medical Electronics Co.. The 510(k) number is K910624.

When did CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 receive FDA 510(k) clearance?

CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 received FDA 510(k) clearance on 1992-01-17, under 510(k) number K910624.

Who is the listed applicant for CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4?

The FDA 510(k) record lists Wr Medical Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4?

The FDA product code for CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 is LLN.

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Other records listing Wr Medical Electronics Co. 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.

K092809HRV ACQUIREK063560HILGER DUAL-STIM NERVE STIMULATORK000574IONTOPHORETIC DRUG DELIVERY ELECTRODE, IONTOPHORETIC ELECTRODE (ACTIVE)K992874Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEMK895838BRACKMANN EMG MONITORING SYSTEM

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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