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FDA 510(k)

MODEL 1750 STANDING URINAL

K-Number: K790663 · 1979-04-24

ApplicantLife-Tech Instruments, Inc.
Decision Date1979-04-24
Product CodeFFG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 1750 STANDING URINAL 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 1979-04-24 under 510(k) number K790663. The device is classified under product code FFG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1750 STANDING URINAL?

MODEL 1750 STANDING URINAL is a medical device that received FDA 510(k) clearance on 1979-04-24. The listed applicant is Life-Tech Instruments, Inc.. The 510(k) number is K790663.

When did MODEL 1750 STANDING URINAL receive FDA 510(k) clearance?

MODEL 1750 STANDING URINAL received FDA 510(k) clearance on 1979-04-24, under 510(k) number K790663.

Who is the listed applicant for MODEL 1750 STANDING URINAL?

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 MODEL 1750 STANDING URINAL?

The FDA product code for MODEL 1750 STANDING URINAL is FFG.

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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 MODULEK812179LIFE-TECH #1753 BIOFEEDBACK TRAINERK812180LIFE-TECH #5102 VISULABK812178LIFE-TECH #'S 1106/1156 UROLABSK800112AMBLYOPIA TRAINERK790664MODEL 1309 AUDIO MONITOR

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Related Devices (Code: FFG)

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.

K893827PEAK FLOW RATE METERLaytech Medical Co.K883274SURGITEK (R) UROFLOW SYSTEMMedical Engineering Corp.K850169ERIS URO-DIAGNOSTIC SYSTEMEris Medical TechnologyK8443381URO-LOG HOME DIAGNOSTIC PACKEpcom Medical Systems, Inc.K843442URINARY DRAINAGE CONTAINER 2013 WITHVital Metrics, Inc.K843441URINARY DRAINAGE CONTAINER 2012-WITHVital Metrics, Inc.

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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