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FDA 510(k)

PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F

K-Number: K960715 · 1996-09-09

ApplicantIdeas For Medicine, Inc.
Decision Date1996-09-09
Product CodeMJN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F 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 1996-09-09 under 510(k) number K960715. 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-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F?

PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F is a medical device that received FDA 510(k) clearance on 1996-09-09. The listed applicant is Ideas For Medicine, Inc.. The 510(k) number is K960715.

When did PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F receive FDA 510(k) clearance?

PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F received FDA 510(k) clearance on 1996-09-09, under 510(k) number K960715.

Who is the listed applicant for PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F?

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-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F?

The FDA product code for PRUITT-INAHARA CAROTID SHUNT 400-40-8F/INAHARA-PRUITT CAROTID SHUNT 500-50-8F is MJN.

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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 CATHETEK960422PRUITT SAFETY OCCLUSION CATHETERK954713DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION)K935964IDEAS OCCLUDER

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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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