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FDA 510(k)

URINARY DRAINAGE UNT

K-Number: K802664 · 1980-11-12

Decision Date1980-11-12
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY DRAINAGE UNT is the device name listed in this FDA 510(k) record. The listed applicant is Diamed Division Ill. Tool Works, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802664. 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 UNT?

URINARY DRAINAGE UNT is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Diamed Division Ill. Tool Works, Inc.. The 510(k) number is K802664.

When did URINARY DRAINAGE UNT receive FDA 510(k) clearance?

URINARY DRAINAGE UNT received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802664.

Who is the listed applicant for URINARY DRAINAGE UNT?

The FDA 510(k) record lists Diamed Division Ill. Tool Works, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URINARY DRAINAGE UNT?

The FDA product code for URINARY DRAINAGE UNT 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 Diamed Division Ill. Tool Works, 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 7 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

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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