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FDA 510(k)

URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR

K-Number: K903816 · 1990-10-31

ApplicantRespiratory Support Products, Inc.
Decision Date1990-10-31
Product CodeEZK
Advisory CommitteeGU
DecisionUnknown

Device Summary

URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K903816. The device is classified under product code EZK. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR?

URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K903816.

When did URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR receive FDA 510(k) clearance?

URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR received FDA 510(k) clearance on 1990-10-31, under 510(k) number K903816.

Who is the listed applicant for URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR?

The FDA 510(k) record lists Respiratory Support Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR?

The FDA product code for URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR is EZK.

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Other records listing Respiratory Support Products, 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.

K983862CLOUD 1 HUMIDIFICATION SYSTEMK921190ADAP-TEMP TEMPERATURE SENSOR ADAPTERK920469MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIEK921510GAS SAMPLING KIT MODIFICATIONK913082BI-TEMP TEMPERATURE MONITOR,MODEL TM-300DK913083BI-TEMP TEMPERATURE MONITOR TM-201D

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Related Devices (Code: EZK)

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.

K911349E-Z-EM ENTEROCLYSIS CATHETER SETE-Z-Em, Inc.K770408KARAYA GUM POWDER, OSTOMYHowmedica 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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