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FDA 510(k)

N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE)

K-Number: K864177 · 1987-02-24

ApplicantCls Co.
Decision Date1987-02-24
Product CodeJXA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE) is the device name listed in this FDA 510(k) record. The listed applicant is Cls Co.. It received FDA 510(k) clearance on 1987-02-24 under 510(k) number K864177. The device is classified under product code JXA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE)?

N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE) is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is Cls Co.. The 510(k) number is K864177.

When did N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE) receive FDA 510(k) clearance?

N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE) received FDA 510(k) clearance on 1987-02-24, under 510(k) number K864177.

Who is the listed applicant for N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE)?

The FDA 510(k) record lists Cls Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE)?

The FDA product code for N-D URINE TUBE SYSTEM (N-D TUBE/CAP/PIPETTE) is JXA.

Related Clinical Trials

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.

Related Devices (Code: JXA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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