FDA 510(k)

VASCULAR CLAMP

K-Number: K881158 · 1988-06-20

ApplicantT. Korossurgical Instruments Corp.

Decision Date1988-06-20

Product CodeDXC

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VASCULAR CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1988-06-20 under 510(k) number K881158. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR CLAMP?

VASCULAR CLAMP is a medical device that received FDA 510(k) clearance on 1988-06-20. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K881158.

When did VASCULAR CLAMP receive FDA 510(k) clearance?

VASCULAR CLAMP received FDA 510(k) clearance on 1988-06-20, under 510(k) number K881158.

Who is the listed applicant for VASCULAR CLAMP?

The FDA 510(k) record lists T. Korossurgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCULAR CLAMP?

The FDA product code for VASCULAR CLAMP is DXC.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.