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FDA 510(k)

URINARY DRAINAGE SET, CLOSED, STERILE

K-Number: K770320 · 1977-03-16

Decision Date1977-03-16
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY DRAINAGE SET, CLOSED, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1977-03-16 under 510(k) number K770320. 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 URINARY DRAINAGE SET, CLOSED, STERILE?

URINARY DRAINAGE SET, CLOSED, STERILE is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is Medical Devices, Inc.. The 510(k) number is K770320.

When did URINARY DRAINAGE SET, CLOSED, STERILE receive FDA 510(k) clearance?

URINARY DRAINAGE SET, CLOSED, STERILE received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770320.

Who is the listed applicant for URINARY DRAINAGE SET, CLOSED, STERILE?

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

What is the FDA product code for URINARY DRAINAGE SET, CLOSED, STERILE?

The FDA product code for URINARY DRAINAGE SET, CLOSED, STERILE 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 Medical Devices, 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.

View all 49 devices →

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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