FDA 510(k)

URETHAL CUTTER CLAMP

K-Number: K820015 · 1982-02-22

ApplicantLone Star Medical Products, Inc.

Decision Date1982-02-22

Product CodeKOA

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

URETHAL CUTTER CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Lone Star Medical Products, Inc.. It received FDA 510(k) clearance on 1982-02-22 under 510(k) number K820015. 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 URETHAL CUTTER CLAMP?

URETHAL CUTTER CLAMP is a medical device that received FDA 510(k) clearance on 1982-02-22. The listed applicant is Lone Star Medical Products, Inc.. The 510(k) number is K820015.

When did URETHAL CUTTER CLAMP receive FDA 510(k) clearance?

URETHAL CUTTER CLAMP received FDA 510(k) clearance on 1982-02-22, under 510(k) number K820015.

Who is the listed applicant for URETHAL CUTTER CLAMP?

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

What is the FDA product code for URETHAL CUTTER CLAMP?

The FDA product code for URETHAL CUTTER CLAMP is KOA.

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Other records listing Lone Star Medical Products, Inc. as applicant

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Related Devices (Code: KOA)

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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.