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FDA 510(k)

REUSABLE CANNULA

K-Number: K002542 · 2000-10-23

ApplicantGenicon, LC
Decision Date2000-10-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REUSABLE CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Genicon, LC. It received FDA 510(k) clearance on 2000-10-23 under 510(k) number K002542. 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 REUSABLE CANNULA?

REUSABLE CANNULA is a medical device that received FDA 510(k) clearance on 2000-10-23. The listed applicant is Genicon, LC. The 510(k) number is K002542.

When did REUSABLE CANNULA receive FDA 510(k) clearance?

REUSABLE CANNULA received FDA 510(k) clearance on 2000-10-23, under 510(k) number K002542.

Who is the listed applicant for REUSABLE CANNULA?

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

What is the FDA product code for REUSABLE CANNULA?

The FDA product code for REUSABLE CANNULA is GCJ.

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Other records listing Genicon, LC 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.

K030174GENICON LAPAROSCOPESK030269GENICON CLIP APPLIERK993625INSUFFLATION NEEDLE- 120MM, MODEL 900-200K991382SHIELDEDTROCAR/CANNULA SYSTEM, MODEL 101-005-101K982472GENICON TROCAR

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

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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