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FDA 510(k)

GODAT UTERINE MANIPULATOR INJECTOR

K-Number: K935023 · 1995-01-04

ApplicantIdeas For Medicine, Inc.
Decision Date1995-01-04
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GODAT UTERINE MANIPULATOR INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Ideas For Medicine, Inc.. It received FDA 510(k) clearance on 1995-01-04 under 510(k) number K935023. 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 GODAT UTERINE MANIPULATOR INJECTOR?

GODAT UTERINE MANIPULATOR INJECTOR is a medical device that received FDA 510(k) clearance on 1995-01-04. The listed applicant is Ideas For Medicine, Inc.. The 510(k) number is K935023.

When did GODAT UTERINE MANIPULATOR INJECTOR receive FDA 510(k) clearance?

GODAT UTERINE MANIPULATOR INJECTOR received FDA 510(k) clearance on 1995-01-04, under 510(k) number K935023.

Who is the listed applicant for GODAT UTERINE MANIPULATOR INJECTOR?

The FDA 510(k) record lists Ideas For Medicine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GODAT UTERINE MANIPULATOR INJECTOR?

The FDA product code for GODAT UTERINE MANIPULATOR INJECTOR is LKF.

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Other records listing Ideas For Medicine, 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.

K961883VERSA-CATH ARTERIAL CATHETERK962751IDEAS' DUAL PORTK961716VASO-SAFE ARTERIAL EMBOLECTOMY CATHETEK960715PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8FK960422PRUITT SAFETY OCCLUSION CATHETERK954713DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION)

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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

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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