FDA 510(k)

DUAL FORCEPLATE

K-Number: K863443 · 1986-09-17

Decision Date1986-09-17

Product CodeKHX

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

DUAL FORCEPLATE is the device name listed in this FDA 510(k) record. The listed applicant is Neurocom International, Inc.. It received FDA 510(k) clearance on 1986-09-17 under 510(k) number K863443. The device is classified under product code KHX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL FORCEPLATE?

DUAL FORCEPLATE is a medical device that received FDA 510(k) clearance on 1986-09-17. The listed applicant is Neurocom International, Inc.. The 510(k) number is K863443.

When did DUAL FORCEPLATE receive FDA 510(k) clearance?

DUAL FORCEPLATE received FDA 510(k) clearance on 1986-09-17, under 510(k) number K863443.

Who is the listed applicant for DUAL FORCEPLATE?

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

What is the FDA product code for DUAL FORCEPLATE?

The FDA product code for DUAL FORCEPLATE is KHX.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Neurocom International, Inc. as applicant

K946229BALANCE MANAGER K901732EMG ACCESSORY FOR POSTUROGRAPHY K871652NEUROCOM PRESSURE TEST SYSTEM K851744EQUITEST

Related Devices (Code: KHX)

K951771COMMUNITY BALANCE PERFORMANCE MONITOR OR COMMUNITY BPMSms Technologies, Ltd.K946229BALANCE MANAGERNeurocom International, Inc.K942694STABILITY SYSTEM (110V) MODEL 945-300; STABILITY SYSTEM (220V) MODEL #945-302Biodex Medical Systems, Inc.K930089SMS BALANCE PERFORMANCE MONITORSms Technologies, Ltd.K921340FORCE MEASURING PLATFORMSra Intl., Inc.K901069COMPUTERIZED FUNCTIONAL TESTING GAIT SYSTEMComputerized Functional Testing Corp.

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.