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FDA 510(k)

UROLOGICAL CATHETER AND ACCESSORIES

K-Number: K925282 · 1993-01-13

Decision Date1993-01-13
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UROLOGICAL CATHETER AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Applied Urology, Inc.. It received FDA 510(k) clearance on 1993-01-13 under 510(k) number K925282. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROLOGICAL CATHETER AND ACCESSORIES?

UROLOGICAL CATHETER AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1993-01-13. The listed applicant is Applied Urology, Inc.. The 510(k) number is K925282.

When did UROLOGICAL CATHETER AND ACCESSORIES receive FDA 510(k) clearance?

UROLOGICAL CATHETER AND ACCESSORIES received FDA 510(k) clearance on 1993-01-13, under 510(k) number K925282.

Who is the listed applicant for UROLOGICAL CATHETER AND ACCESSORIES?

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

What is the FDA product code for UROLOGICAL CATHETER AND ACCESSORIES?

The FDA product code for UROLOGICAL CATHETER AND ACCESSORIES is FAD.

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 Applied Urology, 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 13 devices →

Related Devices (Code: FAD)

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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