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FDA 510(k)

LARIAT LOOP APPLICATOR

K-Number: K060721 · 2006-06-02

ApplicantSentreheart
Decision Date2006-06-02
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LARIAT LOOP APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sentreheart. It received FDA 510(k) clearance on 2006-06-02 under 510(k) number K060721. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARIAT LOOP APPLICATOR?

LARIAT LOOP APPLICATOR is a medical device that received FDA 510(k) clearance on 2006-06-02. The listed applicant is Sentreheart. The 510(k) number is K060721.

When did LARIAT LOOP APPLICATOR receive FDA 510(k) clearance?

LARIAT LOOP APPLICATOR received FDA 510(k) clearance on 2006-06-02, under 510(k) number K060721.

Who is the listed applicant for LARIAT LOOP APPLICATOR?

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

What is the FDA product code for LARIAT LOOP APPLICATOR?

The FDA product code for LARIAT LOOP APPLICATOR is GAT.

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Related Devices (Code: GAT)

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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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