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FDA 510(k)

DMI TOCAR AND CANNULA SYSTEM

K-Number: K926078 · 1993-05-17

ApplicantDiversified Medical Instruments, Inc.
Decision Date1993-05-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DMI TOCAR AND CANNULA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Diversified Medical Instruments, Inc.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K926078. 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 DMI TOCAR AND CANNULA SYSTEM?

DMI TOCAR AND CANNULA SYSTEM is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Diversified Medical Instruments, Inc.. The 510(k) number is K926078.

When did DMI TOCAR AND CANNULA SYSTEM receive FDA 510(k) clearance?

DMI TOCAR AND CANNULA SYSTEM received FDA 510(k) clearance on 1993-05-17, under 510(k) number K926078.

Who is the listed applicant for DMI TOCAR AND CANNULA SYSTEM?

The FDA 510(k) record lists Diversified Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DMI TOCAR AND CANNULA SYSTEM?

The FDA product code for DMI TOCAR AND CANNULA SYSTEM is GCJ.

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Other records listing Diversified Medical Instruments, Inc. 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.

K931814DMI UTERINE MOBILIZER/ELEVATOR/CANNULAK926080DMI LAPAROSCOPIC IRRIGATION PUMPK926079DMI LAPAROSCOPIC ELECTRODES

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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