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FDA 510(k)

CYBERMED, INC., V-WORKS

K-Number: K013878 · 2001-12-07

ApplicantCybermed, Inc.
Decision Date2001-12-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CYBERMED, INC., V-WORKS is the device name listed in this FDA 510(k) record. The listed applicant is Cybermed, Inc.. It received FDA 510(k) clearance on 2001-12-07 under 510(k) number K013878. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYBERMED, INC., V-WORKS?

CYBERMED, INC., V-WORKS is a medical device that received FDA 510(k) clearance on 2001-12-07. The listed applicant is Cybermed, Inc.. The 510(k) number is K013878.

When did CYBERMED, INC., V-WORKS receive FDA 510(k) clearance?

CYBERMED, INC., V-WORKS received FDA 510(k) clearance on 2001-12-07, under 510(k) number K013878.

Who is the listed applicant for CYBERMED, INC., V-WORKS?

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

What is the FDA product code for CYBERMED, INC., V-WORKS?

The FDA product code for CYBERMED, INC., V-WORKS is LLZ.

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Other records listing Cybermed, Inc. as applicant

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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.

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