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FDA 510(k)

LIFE-TECH #1857 PRESSURE/POLOT MODULE

K-Number: K812177 · 1981-09-09

ApplicantLife-Tech Instruments, Inc.
Decision Date1981-09-09
Product CodeEXQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LIFE-TECH #1857 PRESSURE/POLOT MODULE 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 1981-09-09 under 510(k) number K812177. The device is classified under product code EXQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE-TECH #1857 PRESSURE/POLOT MODULE?

LIFE-TECH #1857 PRESSURE/POLOT MODULE is a medical device that received FDA 510(k) clearance on 1981-09-09. The listed applicant is Life-Tech Instruments, Inc.. The 510(k) number is K812177.

When did LIFE-TECH #1857 PRESSURE/POLOT MODULE receive FDA 510(k) clearance?

LIFE-TECH #1857 PRESSURE/POLOT MODULE received FDA 510(k) clearance on 1981-09-09, under 510(k) number K812177.

Who is the listed applicant for LIFE-TECH #1857 PRESSURE/POLOT MODULE?

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 #1857 PRESSURE/POLOT MODULE?

The FDA product code for LIFE-TECH #1857 PRESSURE/POLOT MODULE is EXQ.

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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.

K812179LIFE-TECH #1753 BIOFEEDBACK TRAINERK812180LIFE-TECH #5102 VISULABK812178LIFE-TECH #'S 1106/1156 UROLABSK800112AMBLYOPIA TRAINERK790663MODEL 1750 STANDING URINALK790664MODEL 1309 AUDIO MONITOR

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Related Devices (Code: EXQ)

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.

K253537Glean Urodynamics System Male Delivery System (GUS-1000-M); Glean Urodynamics System Female Delivery System (GUS-1000-F); Glean Urodynamics System Uroflowmeter (UFM-1000 (Uroflowmeter)); Glean Urodynamics System Abdominal Sensor (GUS-1000-A)Bright Uro, Inc.K243052Glean Urodynamics System Male Delivery System (GUS-1000-M); Glean Urodynamics System Female Delivery System (GUS-1000-F); Glean Urodynamics System Uroflowmeter (UFM-1000 (Uroflowmeter))Bright Uro, Inc.K931282VOLUME TRANSDUCERLife-Tech Intl., Inc.K931574ADVANCE MODEL UDS-ADVLaborie Medical Technologies, Ltd.K920574CAMSYS 6300F.M. Wiest USA, Inc.K880391DACOMED CYSTOMETERDacomed Corp.

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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