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FDA 510(k)

MD Mattress Suture Placement Device

K-Number: K222783 · 2024-01-12

Decision Date2024-01-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MD Mattress Suture Placement Device is a medical device manufactured by Lsi Solutions, Inc.. It received FDA 510(k) clearance on 2024-01-12 under approval number K222783. 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 MD Mattress Suture Placement Device?

MD Mattress Suture Placement Device is a medical device that received FDA 510(k) clearance on 2024-01-12. It is manufactured by Lsi Solutions, Inc.. The 510(k) number is K222783.

When was MD Mattress Suture Placement Device approved by the FDA?

MD Mattress Suture Placement Device received FDA 510(k) clearance on 2024-01-12, under approval number K222783.

What company makes MD Mattress Suture Placement Device?

MD Mattress Suture Placement Device is manufactured by Lsi Solutions, Inc..

What is the FDA product code for MD Mattress Suture Placement Device?

The FDA product code for MD Mattress Suture Placement Device is GCJ.

Related Clinical Trials

Other Devices by Lsi Solutions, Inc.

Related Devices (Code: GCJ)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.