FDA 510(k)

CATH-DAP

K-Number: K811277 · 1981-07-20

ApplicantNorthwest Alabama Urological Assoc.

Decision Date1981-07-20

Product CodeKOD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CATH-DAP is the device name listed in this FDA 510(k) record. The listed applicant is Northwest Alabama Urological Assoc.. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811277. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH-DAP?

CATH-DAP is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Northwest Alabama Urological Assoc.. The 510(k) number is K811277.

When did CATH-DAP receive FDA 510(k) clearance?

CATH-DAP received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811277.

Who is the listed applicant for CATH-DAP?

The FDA 510(k) record lists Northwest Alabama Urological Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATH-DAP?

The FDA product code for CATH-DAP is KOD.

Related Devices (Code: KOD)

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.

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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.