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FDA 510(k)

BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30

K-Number: K884850 · 1989-02-02

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

Device Summary

BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 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 K884850. 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 BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30?

BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 is a medical device that received FDA 510(k) clearance on 1989-02-02. The listed applicant is Moe. The 510(k) number is K884850.

When did BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 receive FDA 510(k) clearance?

BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 received FDA 510(k) clearance on 1989-02-02, under 510(k) number K884850.

Who is the listed applicant for BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30?

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 BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30?

The FDA product code for BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 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 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, SYC1K884852BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.K884848BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV

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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