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FDA 510(k)

DMI UTERINE MOBILIZER/ELEVATOR/CANNULA

K-Number: K931814 · 1994-05-31

ApplicantDiversified Medical Instruments, Inc.
Decision Date1994-05-31
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DMI UTERINE MOBILIZER/ELEVATOR/CANNULA 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 1994-05-31 under 510(k) number K931814. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMI UTERINE MOBILIZER/ELEVATOR/CANNULA?

DMI UTERINE MOBILIZER/ELEVATOR/CANNULA is a medical device that received FDA 510(k) clearance on 1994-05-31. The listed applicant is Diversified Medical Instruments, Inc.. The 510(k) number is K931814.

When did DMI UTERINE MOBILIZER/ELEVATOR/CANNULA receive FDA 510(k) clearance?

DMI UTERINE MOBILIZER/ELEVATOR/CANNULA received FDA 510(k) clearance on 1994-05-31, under 510(k) number K931814.

Who is the listed applicant for DMI UTERINE MOBILIZER/ELEVATOR/CANNULA?

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 UTERINE MOBILIZER/ELEVATOR/CANNULA?

The FDA product code for DMI UTERINE MOBILIZER/ELEVATOR/CANNULA is LKF.

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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.

K926080DMI LAPAROSCOPIC IRRIGATION PUMPK926078DMI TOCAR AND CANNULA SYSTEMK926079DMI LAPAROSCOPIC ELECTRODES

Related Devices (Code: LKF)

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.

K253403FemVue® Controlled Saline-Air Device (FSA-300)Femasys, Inc.K252260RELIEEV HSG Catheter (HSG7FA1)Li Medical Corporation , Ltd.K242002FemVue MINI Saline-Air DeviceFemasys, Inc.K240364RELIEEV Uterine Manipulator Injector (CUMI 5.0)Li Medical Corporation , Ltd.K241693FemChec Controlled Saline-Air Device (FCD-250)Femasys, Inc.K222798Rejoni Intrauterine CatheterRejoni, 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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