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Instrumed Vascular Clamps

by Instrumed International, Inc.

510(k) K092544

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK092544 Date26 Oct 2009ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DXC
Device Class
Class II
Regulation
21 CFR Part 870.4450
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

Instrumed Vascular Clamps are surgical instruments designed for the temporary or partial occlusion of blood vessels. These devices are utilized during vascular surgical procedures to control blood flow.

This device is identified under FDA 510(k) clearance number K092544. It is manufactured by Instrumed International, Inc. and is categorized under the cardiovascular advisory committee.

Other devices from Instrumed International, Inc.

Questions

AI-generated answers, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the primary clinical use for Instrumed Vascular Clamps?

    These instruments are designed for the temporary or partial occlusion of blood vessels. They are specifically utilized by surgeons during vascular procedures to effectively control blood flow at the surgical site.

  • What is the regulatory status of these vascular clamps?

    Instrumed Vascular Clamps are cleared for use under FDA 510(k) number K092544. This clearance indicates that the device has been determined to be substantially equivalent to legally marketed predicate devices.

  • Which advisory committee oversees this device category?

    This device is categorized under the cardiovascular advisory committee, which is responsible for reviewing medical devices intended for use in the cardiovascular system.