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FDA 510(k)

DDV LIGATOR

K-Number: K921304 · 1992-10-05

Decision Date1992-10-05
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DDV LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is North American Medical, Inc.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K921304. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DDV LIGATOR?

DDV LIGATOR is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is North American Medical, Inc.. The 510(k) number is K921304.

When did DDV LIGATOR receive FDA 510(k) clearance?

DDV LIGATOR received FDA 510(k) clearance on 1992-10-05, under 510(k) number K921304.

Who is the listed applicant for DDV LIGATOR?

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

What is the FDA product code for DDV LIGATOR?

The FDA product code for DDV LIGATOR is KOA.

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: KOA)

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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