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FDA 510(k)

BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV

K-Number: K884848 · 1989-02-02

ApplicantMoe
Decision Date1989-02-02
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV is the device name listed in this FDA 510(k) record. The listed applicant is Moe. It received FDA 510(k) clearance on 1989-02-02 under 510(k) number K884848. 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 BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV?

BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV is a medical device that received FDA 510(k) clearance on 1989-02-02. The listed applicant is Moe. The 510(k) number is K884848.

When did BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV receive FDA 510(k) clearance?

BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV received FDA 510(k) clearance on 1989-02-02, under 510(k) number K884848.

Who is the listed applicant for BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV?

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

What is the FDA product code for BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV?

The FDA product code for BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV 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.

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 Moe 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.

K884849BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BARK884851BIOFEEDBACK DEVICE TG3, TG4K884853BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1K884850BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30K884852BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.

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

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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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