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FDA 510(k)

LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS

K-Number: K031443 · 2003-06-18

ApplicantLsi Solutions
Decision Date2003-06-18
Product CodeNEW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Solutions. It received FDA 510(k) clearance on 2003-06-18 under 510(k) number K031443. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS?

LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS is a medical device that received FDA 510(k) clearance on 2003-06-18. The listed applicant is Lsi Solutions. The 510(k) number is K031443.

When did LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS receive FDA 510(k) clearance?

LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS received FDA 510(k) clearance on 2003-06-18, under 510(k) number K031443.

Who is the listed applicant for LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS?

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

What is the FDA product code for LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS?

The FDA product code for LSI SOLUTIONS SUTURE QUICK LOAD PRODUCTS is NEW.

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Other records listing Lsi Solutions 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.

K203081RAM COR-SUTURE QUCIK LOAD Surgical Suture, COR-SUTURE QUICK LOAD Surgical SutureK163639LS-5 ePTFE SutureK040232LSI SEW-RIGHT R SERIES SUTURE PLACEMENT DEVICE AND ACCESS PRODUCT SEW-RIGHT SR-5R, MODEL 020999K024301LSI ENDOSCOPIC EXTERNAL ACCESSORY CHANNEL AND ACCESSORIES PRODUCTK011016LSI SOLUTIONS FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES PRODUCTK981531SUTURE PLACEMENT DEVICE AND ACCESSORIES

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Related Devices (Code: NEW)

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.

K254238MINT MONO SuturesHans Biomed CorporationK253879MONOFIX PDOSamyang Holdings CorporationK261988Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical SutureTeleflex Medical, LLCK252171Barbed PDO SutureSutura Medical Technology, Inc.K252047STRATAFIX™ Symmetric PDS™ Plus Knotless Tissue Control DevicesETHICON, Inc.K243897PDS™ Plus Antibacterial (Polydioxanone) Sterile Synthetic Absorbable Surgical SutureETHICON, Inc.

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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