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FDA 510(k)

VENTURI MiNO TG600/14

K-Number: K143004 · 2016-01-05

ApplicantTalley Group, Ltd.
Decision Date2016-01-05
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VENTURI MiNO TG600/14 is the device name listed in this FDA 510(k) record. The listed applicant is Talley Group, Ltd.. It received FDA 510(k) clearance on 2016-01-05 under 510(k) number K143004. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTURI MiNO TG600/14?

VENTURI MiNO TG600/14 is a medical device that received FDA 510(k) clearance on 2016-01-05. The listed applicant is Talley Group, Ltd.. The 510(k) number is K143004.

When did VENTURI MiNO TG600/14 receive FDA 510(k) clearance?

VENTURI MiNO TG600/14 received FDA 510(k) clearance on 2016-01-05, under 510(k) number K143004.

Who is the listed applicant for VENTURI MiNO TG600/14?

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

What is the FDA product code for VENTURI MiNO TG600/14?

The FDA product code for VENTURI MiNO TG600/14 is OMP.

Other records listing Talley Group, Ltd. 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.

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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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