Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV

K-Number: K860914 · 1986-06-06

ApplicantBio-Feedback Systems, Inc.
Decision Date1986-06-06
Product CodeGWK
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Feedback Systems, Inc.. It received FDA 510(k) clearance on 1986-06-06 under 510(k) number K860914. The device is classified under product code GWK. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV?

ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV is a medical device that received FDA 510(k) clearance on 1986-06-06. The listed applicant is Bio-Feedback Systems, Inc.. The 510(k) number is K860914.

When did ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV receive FDA 510(k) clearance?

ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV received FDA 510(k) clearance on 1986-06-06, under 510(k) number K860914.

Who is the listed applicant for ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV?

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

What is the FDA product code for ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV?

The FDA product code for ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV is GWK.

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 Bio-Feedback Systems, 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.

K905372MINIATURE ELECTRODERMAL RESPONSE TRAINER EDR-002K905373MINIATURE TEMPERATURE TRAINER MODEL DT-002K900063MULTI-CHANNEL ISOLATION AMPLIFIER (MCIA)K832333FEEDBACK EMG SYSTEM PE-020K812619ISOLATED VOLTAGE/FREQUENCY CONVERTERK792659FEEDBACK EDR SYSTEM MODEL ME-1

View all 11 devices →

Related Devices (Code: GWK)

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.

K060919ACTICALRespironics, Inc.K061870VITALSENSE XHRRespironics, Inc.K052489ACTIHEARTRespironics, Inc.K991045MINI-LOGGER SERIES 2000Mini-Mitter Co., Inc.K905594NEUROFILE DATA STORAGE/ACCESORIES TO THE EEG-4300Nihon Kohden America, Inc.K904328VISTA POLYSOMNOGRAPHY COMPUTER SYSTEMTelediagnostic 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.

↑