FDA 510(k)

VCS-A SERIES CLAMP

K-Number: K011863 · 2002-02-15

Decision Date2002-02-15

Product CodeDXC

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VCS-A SERIES CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Control Systems, Inc.. It received FDA 510(k) clearance on 2002-02-15 under 510(k) number K011863. 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 VCS-A SERIES CLAMP?

VCS-A SERIES CLAMP is a medical device that received FDA 510(k) clearance on 2002-02-15. The listed applicant is Vascular Control Systems, Inc.. The 510(k) number is K011863.

When did VCS-A SERIES CLAMP receive FDA 510(k) clearance?

VCS-A SERIES CLAMP received FDA 510(k) clearance on 2002-02-15, under 510(k) number K011863.

Who is the listed applicant for VCS-A SERIES CLAMP?

The FDA 510(k) record lists Vascular Control Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VCS-A SERIES CLAMP?

The FDA product code for VCS-A SERIES CLAMP is DXC.

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Other records listing Vascular Control Systems, Inc. as applicant

K060573BURBANK TENACULUM K052209VCS DOPPLER TRANSCEIVER, MODEL 09-0023-01 K032125CSTAT, MODELS 09-0014-01 AND 09-0014-02 K031812TRANSVAGINAL DOPPLER CLAMP, MODELS: 09-0016-01, 09-0016-02, 09-0016-03 K031358TRANSVAGINAL DOPPLER PROBE K030078BURBANK TENACULUM, MODEL 09-0011-01

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Related Devices (Code: DXC)

K262086PreludeSYNC™ Radial Compression DeviceMerit Medical Systems, Inc.K260105Fogarty Spring Clips, Handleless Clamps, and Clamp InsertsEdwards Lifesciences K252772Arc Adjustable Radial Cuff Compression DeviceTz Medical, Inc.K254060Life Saving TourniquetTW Medical K243627Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)Arc Trauma, LLC K253070Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)Medline Industries, LP

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.