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FDA 510(k)

DILECTRON URINARY CONDUCTIVITY PROBE

K-Number: K891681 · 1990-05-01

ApplicantGyrus Medical , Ltd.
Decision Date1990-05-01
Product CodeJRE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DILECTRON URINARY CONDUCTIVITY PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Medical , Ltd.. It received FDA 510(k) clearance on 1990-05-01 under 510(k) number K891681. The device is classified under product code JRE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DILECTRON URINARY CONDUCTIVITY PROBE?

DILECTRON URINARY CONDUCTIVITY PROBE is a medical device that received FDA 510(k) clearance on 1990-05-01. The listed applicant is Gyrus Medical , Ltd.. The 510(k) number is K891681.

When did DILECTRON URINARY CONDUCTIVITY PROBE receive FDA 510(k) clearance?

DILECTRON URINARY CONDUCTIVITY PROBE received FDA 510(k) clearance on 1990-05-01, under 510(k) number K891681.

Who is the listed applicant for DILECTRON URINARY CONDUCTIVITY PROBE?

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

What is the FDA product code for DILECTRON URINARY CONDUCTIVITY PROBE?

The FDA product code for DILECTRON URINARY CONDUCTIVITY PROBE is JRE.

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Other records listing Gyrus Medical , 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.

K041285GYRUS G3 SYSTEM (GENERATOR, ASSESSORIES, SOMNOPLASTY ELECTRODES AND PLASMACISION ELECTRODES)K003569PLASMAKINETIC ENDOUROLOGY SYSTEMK001270GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE LOOP ELECTRODEK994166GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE ELECTRODEK993749GYRUS HYSTEROSCOPIC RESECTOSCOPEK990628GYRUS ENDOUROLOGY SYSTEM

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Related Devices (Code: JRE)

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.

K954977URINE REAGENTS STRIPS-8 PARAMETERS (MODIFICATION)Teco DiagnosticsK941906MODEL 2730 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941903MODEL 2740 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941901MODEL 2721 CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941904MODEL A300CL CLINICAL REFRACTOMETERVee Gee Scientific, Inc.K941905MODEL 3461 CLINICAL REFRACTOMETERVee Gee Scientific, 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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