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FDA 510(k)

LIFE-TECH #1753 BIOFEEDBACK TRAINER

K-Number: K812179 · 1981-08-25

ApplicantLife-Tech Instruments, Inc.
Decision Date1981-08-25
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LIFE-TECH #1753 BIOFEEDBACK TRAINER is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Instruments, Inc.. It received FDA 510(k) clearance on 1981-08-25 under 510(k) number K812179. 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 LIFE-TECH #1753 BIOFEEDBACK TRAINER?

LIFE-TECH #1753 BIOFEEDBACK TRAINER is a medical device that received FDA 510(k) clearance on 1981-08-25. The listed applicant is Life-Tech Instruments, Inc.. The 510(k) number is K812179.

When did LIFE-TECH #1753 BIOFEEDBACK TRAINER receive FDA 510(k) clearance?

LIFE-TECH #1753 BIOFEEDBACK TRAINER received FDA 510(k) clearance on 1981-08-25, under 510(k) number K812179.

Who is the listed applicant for LIFE-TECH #1753 BIOFEEDBACK TRAINER?

The FDA 510(k) record lists Life-Tech Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFE-TECH #1753 BIOFEEDBACK TRAINER?

The FDA product code for LIFE-TECH #1753 BIOFEEDBACK TRAINER is HCC.

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Other records listing Life-Tech Instruments, 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.

K812177LIFE-TECH #1857 PRESSURE/POLOT MODULEK812180LIFE-TECH #5102 VISULABK812178LIFE-TECH #'S 1106/1156 UROLABSK800112AMBLYOPIA TRAINERK790663MODEL 1750 STANDING URINALK790664MODEL 1309 AUDIO MONITOR

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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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