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FDA 510(k)

PRUITT SAFETY OCCLUSION CATHETER

K-Number: K960422 · 1996-08-07

ApplicantIdeas For Medicine, Inc.
Decision Date1996-08-07
Product CodeMJN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRUITT SAFETY OCCLUSION CATHETER 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 1996-08-07 under 510(k) number K960422. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRUITT SAFETY OCCLUSION CATHETER?

PRUITT SAFETY OCCLUSION CATHETER is a medical device that received FDA 510(k) clearance on 1996-08-07. The listed applicant is Ideas For Medicine, Inc.. The 510(k) number is K960422.

When did PRUITT SAFETY OCCLUSION CATHETER receive FDA 510(k) clearance?

PRUITT SAFETY OCCLUSION CATHETER received FDA 510(k) clearance on 1996-08-07, under 510(k) number K960422.

Who is the listed applicant for PRUITT SAFETY OCCLUSION CATHETER?

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 PRUITT SAFETY OCCLUSION CATHETER?

The FDA product code for PRUITT SAFETY OCCLUSION CATHETER is MJN.

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 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 500-50-8FK954713DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION)K935964IDEAS OCCLUDER

View all 15 devices →

Related Devices (Code: MJN)

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.

K243795pREBOA-PRO CatheterPrytime Medical Devices, Inc.K251358Bridge Plus Occlusion Balloon (590-002)Philips Image Guided Therapy DevicesK221294preCARDIA Occlusion SystemAbiomed, Inc.K214060LANDMARK REBOA CatheterZien Medical Technologies, Inc.K211610Fogarty Occlusion CatheterEdwards Lifesciences, LLCK212324RenovoCathRenovorx, 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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