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FDA 510(k)

VENDYS, MODEL 6000 B B/C

K-Number: K072919 · 2007-11-02

ApplicantEndothelix, Inc.
Decision Date2007-11-02
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VENDYS, MODEL 6000 B B/C is the device name listed in this FDA 510(k) record. The listed applicant is Endothelix, Inc.. It received FDA 510(k) clearance on 2007-11-02 under 510(k) number K072919. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENDYS, MODEL 6000 B B/C?

VENDYS, MODEL 6000 B B/C is a medical device that received FDA 510(k) clearance on 2007-11-02. The listed applicant is Endothelix, Inc.. The 510(k) number is K072919.

When did VENDYS, MODEL 6000 B B/C receive FDA 510(k) clearance?

VENDYS, MODEL 6000 B B/C received FDA 510(k) clearance on 2007-11-02, under 510(k) number K072919.

Who is the listed applicant for VENDYS, MODEL 6000 B B/C?

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

What is the FDA product code for VENDYS, MODEL 6000 B B/C?

The FDA product code for VENDYS, MODEL 6000 B B/C is DQK.

Related Clinical Trials

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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Other records listing Endothelix, Inc. as applicant

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.

K060980VENDYS MODEL 5000 B/BC

Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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.

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