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FDA 510(k)

ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM

K-Number: K061555 · 2006-08-31

ApplicantAnchor Products Co.
Decision Date2006-08-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Anchor Products Co.. It received FDA 510(k) clearance on 2006-08-31 under 510(k) number K061555. 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 ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM?

ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM is a medical device that received FDA 510(k) clearance on 2006-08-31. The listed applicant is Anchor Products Co.. The 510(k) number is K061555.

When did ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM receive FDA 510(k) clearance?

ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM received FDA 510(k) clearance on 2006-08-31, under 510(k) number K061555.

Who is the listed applicant for ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM?

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

What is the FDA product code for ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM?

The FDA product code for ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM is GCJ.

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Other records listing Anchor Products Co. 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.

K091930ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SBK982073ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEMK884862ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADEK873124ANCHOR BIOPSY NEEDLEK831648ANCHOR BRAND SURGICAL NEEDLESK790405ANCHOR BRAND COUNT-TAINER

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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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