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FDA 510(k)

TEMP. & GSR BIOFEEDBACK DEVICE

K-Number: K842023 · 1984-07-20

ApplicantElectronics Research & Production
Decision Date1984-07-20
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TEMP. & GSR BIOFEEDBACK DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Electronics Research & Production. It received FDA 510(k) clearance on 1984-07-20 under 510(k) number K842023. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP. & GSR BIOFEEDBACK DEVICE?

TEMP. & GSR BIOFEEDBACK DEVICE is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is Electronics Research & Production. The 510(k) number is K842023.

When did TEMP. & GSR BIOFEEDBACK DEVICE receive FDA 510(k) clearance?

TEMP. & GSR BIOFEEDBACK DEVICE received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842023.

Who is the listed applicant for TEMP. & GSR BIOFEEDBACK DEVICE?

The FDA 510(k) record lists Electronics Research & Production as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMP. & GSR BIOFEEDBACK DEVICE?

The FDA product code for TEMP. & GSR BIOFEEDBACK DEVICE is HCC.

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.

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Other records listing Electronics Research & Production 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.

K842021EEG BIOFEEDBACK DEVICE ACCESSORYK842022EEG BIOFEEDBACK DEVICE

Related Devices (Code: HCC)

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.

K233580A Breathing System (ABS)Deepwell Dtx, Inc.K222101PrismGraymatters Health , Ltd.K180173FreespiraPalo Alto Health Sciences, Inc.K163448GrindCare SystemSunstar Suisse S.A.K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.K122879EEGER4 MODEL 4.3Eeg Software, LLC

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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