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FDA 510(k)

ACCUMETER ELECTRONIC URINEMETER SYSTEM

K-Number: K844030 · 1984-11-20

ApplicantTravenol Laboratories, S.A.
Decision Date1984-11-20
Product CodeFFG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACCUMETER ELECTRONIC URINEMETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1984-11-20 under 510(k) number K844030. 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 ACCUMETER ELECTRONIC URINEMETER SYSTEM?

ACCUMETER ELECTRONIC URINEMETER SYSTEM is a medical device that received FDA 510(k) clearance on 1984-11-20. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K844030.

When did ACCUMETER ELECTRONIC URINEMETER SYSTEM receive FDA 510(k) clearance?

ACCUMETER ELECTRONIC URINEMETER SYSTEM received FDA 510(k) clearance on 1984-11-20, under 510(k) number K844030.

Who is the listed applicant for ACCUMETER ELECTRONIC URINEMETER SYSTEM?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCUMETER ELECTRONIC URINEMETER SYSTEM?

The FDA product code for ACCUMETER ELECTRONIC URINEMETER SYSTEM is FFG.

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Other records listing Travenol Laboratories, S.A. 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.

K874181BAXTER BEDSIDE SYSTEMK873894CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITEK873873RESUBMITTED MICRON TRANSFUSION FILTERK873984AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)K872364HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309K872652UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM

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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.K843441URINARY DRAINAGE CONTAINER 2012-WITHVital Metrics, Inc.K843442URINARY DRAINAGE CONTAINER 2013 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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