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FDA 510(k)

RIMECO MIDSTREAM URINE COLLECTOR

K-Number: K943752 · 1994-11-01

ApplicantRimeco Products, Inc.
Decision Date1994-11-01
Product CodeFOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RIMECO MIDSTREAM URINE COLLECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Rimeco Products, Inc.. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K943752. The device is classified under product code FOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIMECO MIDSTREAM URINE COLLECTOR?

RIMECO MIDSTREAM URINE COLLECTOR is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Rimeco Products, Inc.. The 510(k) number is K943752.

When did RIMECO MIDSTREAM URINE COLLECTOR receive FDA 510(k) clearance?

RIMECO MIDSTREAM URINE COLLECTOR received FDA 510(k) clearance on 1994-11-01, under 510(k) number K943752.

Who is the listed applicant for RIMECO MIDSTREAM URINE COLLECTOR?

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

What is the FDA product code for RIMECO MIDSTREAM URINE COLLECTOR?

The FDA product code for RIMECO MIDSTREAM URINE COLLECTOR is FOC.

Related Clinical Trials

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Related Devices (Code: FOC)

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.

K950176PREMIE U-BAG URINE SPECIMEN COLLECTORHollister, Inc.K911329BARD(R) SURECATCH PEDIATRIC URINE COLLECT DEVICEC.R. Bard, Inc.K771368PORTABLE INFANT VENTILATORCavitron 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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