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FDA 510(k)

REUSABLE TROCAR WITH SLEEVE (COMMON)

K-Number: K963815 · 1996-11-05

ApplicantPilling Weck Group
Decision Date1996-11-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REUSABLE TROCAR WITH SLEEVE (COMMON) is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Weck Group. It received FDA 510(k) clearance on 1996-11-05 under 510(k) number K963815. 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 TROCAR WITH SLEEVE (COMMON)?

REUSABLE TROCAR WITH SLEEVE (COMMON) is a medical device that received FDA 510(k) clearance on 1996-11-05. The listed applicant is Pilling Weck Group. The 510(k) number is K963815.

When did REUSABLE TROCAR WITH SLEEVE (COMMON) receive FDA 510(k) clearance?

REUSABLE TROCAR WITH SLEEVE (COMMON) received FDA 510(k) clearance on 1996-11-05, under 510(k) number K963815.

Who is the listed applicant for REUSABLE TROCAR WITH SLEEVE (COMMON)?

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

What is the FDA product code for REUSABLE TROCAR WITH SLEEVE (COMMON)?

The FDA product code for REUSABLE TROCAR WITH SLEEVE (COMMON) 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 Pilling Weck Group 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.

K971334PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCARK965176PILLING WECK 2 PIECE TAKE-APART INSTRUMENTSK964450SECONDARY TROCAR AND SLEEVE WITH INSUFFLATION PORTK964123REUSABLE TROCAR WITH SLEEVE (COMMON)

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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