Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX

K-Number: K001597 · 2000-06-05

ApplicantConmedcorp
Decision Date2000-06-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 2000-06-05 under 510(k) number K001597. 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 CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX?

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX is a medical device that received FDA 510(k) clearance on 2000-06-05. The listed applicant is Conmedcorp. The 510(k) number is K001597.

When did CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX receive FDA 510(k) clearance?

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX received FDA 510(k) clearance on 2000-06-05, under 510(k) number K001597.

Who is the listed applicant for CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX?

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

What is the FDA product code for CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX?

The FDA product code for CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Conmedcorp 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.

K101534CONMED ALTRUS THERMAL TISSUE FUSION SYSTEMK061021ENTAKE STANDARD AND SAFETY PEG SYSTEMK050992CONMED IRRIGATION NOZZLEK050777PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907K050304FX WIRE ADVANCED MEASUREMENT GUIDEWIREK041953VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART

View all 92 devices →

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.

↑