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FDA 510(k)

ZMED VP4000

K-Number: K130929 · 2013-04-12

ApplicantZmed, Inc.
Decision Date2013-04-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ZMED VP4000 is the device name listed in this FDA 510(k) record. The listed applicant is Zmed, Inc.. It received FDA 510(k) clearance on 2013-04-12 under 510(k) number K130929. 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 ZMED VP4000?

ZMED VP4000 is a medical device that received FDA 510(k) clearance on 2013-04-12. The listed applicant is Zmed, Inc.. The 510(k) number is K130929.

When did ZMED VP4000 receive FDA 510(k) clearance?

ZMED VP4000 received FDA 510(k) clearance on 2013-04-12, under 510(k) number K130929.

Who is the listed applicant for ZMED VP4000?

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

What is the FDA product code for ZMED VP4000?

The FDA product code for ZMED VP4000 is LLZ.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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