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FDA 510(k)

NICKI, MODEL NUMBER USD-NK-UP1

K-Number: K924086 · 1992-10-20

ApplicantLaborie Medical Technologies, Ltd.
Decision Date1992-10-20
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NICKI, MODEL NUMBER USD-NK-UP1 is the device name listed in this FDA 510(k) record. The listed applicant is Laborie Medical Technologies, Ltd.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K924086. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICKI, MODEL NUMBER USD-NK-UP1?

NICKI, MODEL NUMBER USD-NK-UP1 is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is Laborie Medical Technologies, Ltd.. The 510(k) number is K924086.

When did NICKI, MODEL NUMBER USD-NK-UP1 receive FDA 510(k) clearance?

NICKI, MODEL NUMBER USD-NK-UP1 received FDA 510(k) clearance on 1992-10-20, under 510(k) number K924086.

Who is the listed applicant for NICKI, MODEL NUMBER USD-NK-UP1?

The FDA 510(k) record lists Laborie Medical Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NICKI, MODEL NUMBER USD-NK-UP1?

The FDA product code for NICKI, MODEL NUMBER USD-NK-UP1 is FAP.

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Other records listing Laborie Medical Technologies, Ltd. 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.

K090830LABORIE INJETAK ADJUSTABLE TIP NEEDLE, FLEXIBLE TIP AND RIDGID TIPK962009UROSTYMK955856TEX-AID BLUEK955810U-TEXK951805PIPER, MODEL NUMBER UDS-PIPERBK942563ELITE BIOFEEDBACK

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Related Devices (Code: FAP)

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.

K113771SIGNAL GEAR URETHRAL CATHETER ELECTRODENeurovision Medical Products, Inc.K974775SINGLE CHANNEL UROLOGICAL PRESSURE GAUGE, DUAL CHANNEL UROLOGICAL PRESSURE GAUGEAirtronic Services, Inc.K963330URODYNAMIC ANALYSIS MODULESynectics Medical, Inc.K962472RUSCH URODYNAMIC RECTAL BALLOON 2-WAY CATHETERRusch Intl.K931175SCHUSTER DISPOSABLE BALLOON PROBESandhill Scientific, Inc.K931179UROLAB SPECTRUMLife-Tech Intl., 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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