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)

DMI LAPAROSCOPIC ELECTRODES

K-Number: K926079 · 1993-04-07

ApplicantDiversified Medical Instruments, Inc.
Decision Date1993-04-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DMI LAPAROSCOPIC ELECTRODES 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 1993-04-07 under 510(k) number K926079. 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 ELECTRODES?

DMI LAPAROSCOPIC ELECTRODES is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Diversified Medical Instruments, Inc.. The 510(k) number is K926079.

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

DMI LAPAROSCOPIC ELECTRODES received FDA 510(k) clearance on 1993-04-07, under 510(k) number K926079.

Who is the listed applicant for DMI LAPAROSCOPIC ELECTRODES?

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 ELECTRODES?

The FDA product code for DMI LAPAROSCOPIC ELECTRODES 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 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 PUMPK926078DMI TOCAR AND CANNULA SYSTEM

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.

↑