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FDA 510(k)

MULTIPLE SYS-URINE DRAINAGE-CLOSED

K-Number: K840284 · 1984-04-13

ApplicantLuth Corp.
Decision Date1984-04-13
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MULTIPLE SYS-URINE DRAINAGE-CLOSED is the device name listed in this FDA 510(k) record. The listed applicant is Luth Corp.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840284. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE SYS-URINE DRAINAGE-CLOSED?

MULTIPLE SYS-URINE DRAINAGE-CLOSED is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Luth Corp.. The 510(k) number is K840284.

When did MULTIPLE SYS-URINE DRAINAGE-CLOSED receive FDA 510(k) clearance?

MULTIPLE SYS-URINE DRAINAGE-CLOSED received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840284.

Who is the listed applicant for MULTIPLE SYS-URINE DRAINAGE-CLOSED?

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

What is the FDA product code for MULTIPLE SYS-URINE DRAINAGE-CLOSED?

The FDA product code for MULTIPLE SYS-URINE DRAINAGE-CLOSED is KNX.

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.

Other records listing Luth Corp. 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.

Related Devices (Code: KNX)

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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