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FDA 510(k)

DISPOSABLE SUTURE PLACEMENT SYSTEM

K-Number: K932553 · 1994-05-12

ApplicantLaurus Medical Corp.
Decision Date1994-05-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SUTURE PLACEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Laurus Medical Corp.. It received FDA 510(k) clearance on 1994-05-12 under 510(k) number K932553. 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 DISPOSABLE SUTURE PLACEMENT SYSTEM?

DISPOSABLE SUTURE PLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1994-05-12. The listed applicant is Laurus Medical Corp.. The 510(k) number is K932553.

When did DISPOSABLE SUTURE PLACEMENT SYSTEM receive FDA 510(k) clearance?

DISPOSABLE SUTURE PLACEMENT SYSTEM received FDA 510(k) clearance on 1994-05-12, under 510(k) number K932553.

Who is the listed applicant for DISPOSABLE SUTURE PLACEMENT SYSTEM?

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

What is the FDA product code for DISPOSABLE SUTURE PLACEMENT SYSTEM?

The FDA product code for DISPOSABLE SUTURE PLACEMENT SYSTEM is GCJ.

Related Clinical Trials

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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Other records listing Laurus Medical Corp. 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.

K973415CURVILINEAR SUTURE PLACEMENT SYSTEMK973215STEREOTACTIC NEEDLE CORE BIOPSY SYSTEMK960317LAURUS NEEDLE CORE BIOPSY SYSTEM

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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.

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