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FDA 510(k)

ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT

K-Number: K926110 · 1993-07-08

ApplicantAdvanced Surgical Intervention, Inc.
Decision Date1993-07-08
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical Intervention, Inc.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K926110. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT?

ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Advanced Surgical Intervention, Inc.. The 510(k) number is K926110.

When did ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT receive FDA 510(k) clearance?

ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT received FDA 510(k) clearance on 1993-07-08, under 510(k) number K926110.

Who is the listed applicant for ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT?

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

What is the FDA product code for ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT?

The FDA product code for ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT is GCJ.

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Related Devices (Code: GCJ)

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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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