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FDA 510(k)

DMI LAPAROSCOPIC IRRIGATION PUMP

K-Number: K926080 · 1994-02-25

ApplicantDiversified Medical Instruments, Inc.
Decision Date1994-02-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DMI LAPAROSCOPIC IRRIGATION PUMP 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 1994-02-25 under 510(k) number K926080. 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 LAPAROSCOPIC IRRIGATION PUMP?

DMI LAPAROSCOPIC IRRIGATION PUMP is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Diversified Medical Instruments, Inc.. The 510(k) number is K926080.

When did DMI LAPAROSCOPIC IRRIGATION PUMP receive FDA 510(k) clearance?

DMI LAPAROSCOPIC IRRIGATION PUMP received FDA 510(k) clearance on 1994-02-25, under 510(k) number K926080.

Who is the listed applicant for DMI LAPAROSCOPIC IRRIGATION PUMP?

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 LAPAROSCOPIC IRRIGATION PUMP?

The FDA product code for DMI LAPAROSCOPIC IRRIGATION PUMP 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.

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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/CANNULAK926078DMI TOCAR AND CANNULA SYSTEMK926079DMI 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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