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FDA 510(k)

TRELLIS-8 PERIPHERAL INFUSION SYSTEM

K-Number: K050147 · 2005-02-03

Decision Date2005-02-03
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRELLIS-8 PERIPHERAL INFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bacchus Vascular, Inc.. It received FDA 510(k) clearance on 2005-02-03 under 510(k) number K050147. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRELLIS-8 PERIPHERAL INFUSION SYSTEM?

TRELLIS-8 PERIPHERAL INFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-03. The listed applicant is Bacchus Vascular, Inc.. The 510(k) number is K050147.

When did TRELLIS-8 PERIPHERAL INFUSION SYSTEM receive FDA 510(k) clearance?

TRELLIS-8 PERIPHERAL INFUSION SYSTEM received FDA 510(k) clearance on 2005-02-03, under 510(k) number K050147.

Who is the listed applicant for TRELLIS-8 PERIPHERAL INFUSION SYSTEM?

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

What is the FDA product code for TRELLIS-8 PERIPHERAL INFUSION SYSTEM?

The FDA product code for TRELLIS-8 PERIPHERAL INFUSION SYSTEM is QEY.

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.

Other records listing Bacchus Vascular, 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.

View all 10 devices →

Related Devices (Code: QEY)

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.

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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