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FDA 510(k)

MINIDEF (OR DEFIPORT

K-Number: K823933 · 1983-04-12

ApplicantOdam
Decision Date1983-04-12
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINIDEF (OR DEFIPORT is the device name listed in this FDA 510(k) record. The listed applicant is Odam. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K823933. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIDEF (OR DEFIPORT?

MINIDEF (OR DEFIPORT is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Odam. The 510(k) number is K823933.

When did MINIDEF (OR DEFIPORT receive FDA 510(k) clearance?

MINIDEF (OR DEFIPORT received FDA 510(k) clearance on 1983-04-12, under 510(k) number K823933.

Who is the listed applicant for MINIDEF (OR DEFIPORT?

The FDA 510(k) record lists Odam as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINIDEF (OR DEFIPORT?

The FDA product code for MINIDEF (OR DEFIPORT is LDD.

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 Odam 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.

K972535MAGLIFE CK950264MAGLIFEK854175DEFIGARD 2000K823934CARIEL F12K823931DEFIGARD M(OR DEFISCOPE M

Related Devices (Code: LDD)

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.

K203231Switched Internal PaddlesPhilips North America, LLCK200849Tempus LS - ManualRemote Diagnostic Technologies, Ltd. A Philips CompanyK182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsPhysio-Control, Inc.K103651CARDIOMEDCardio Medical Products, Inc.K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab SpaK103334CARDIO MEDCardio Medical Products, 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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