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FDA 510(k)

URODYNAMIC CATHETERS

K-Number: K923464 · 1993-02-05

Decision Date1993-02-05
Product CodeFAP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URODYNAMIC CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is R.L. Medical Corp.. It received FDA 510(k) clearance on 1993-02-05 under 510(k) number K923464. The device is classified under product code FAP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URODYNAMIC CATHETERS?

URODYNAMIC CATHETERS is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is R.L. Medical Corp.. The 510(k) number is K923464.

When did URODYNAMIC CATHETERS receive FDA 510(k) clearance?

URODYNAMIC CATHETERS received FDA 510(k) clearance on 1993-02-05, under 510(k) number K923464.

Who is the listed applicant for URODYNAMIC CATHETERS?

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

What is the FDA product code for URODYNAMIC CATHETERS?

The FDA product code for URODYNAMIC CATHETERS is FAP.

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: FAP)

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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