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FDA 510(k)

THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT

K-Number: K872090 · 1987-10-30

ApplicantIdeas For Medicine, Inc.
Decision Date1987-10-30
Product CodeDQT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT 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 1987-10-30 under 510(k) number K872090. The device is classified under product code DQT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT?

THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT is a medical device that received FDA 510(k) clearance on 1987-10-30. The listed applicant is Ideas For Medicine, Inc.. The 510(k) number is K872090.

When did THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT receive FDA 510(k) clearance?

THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT received FDA 510(k) clearance on 1987-10-30, under 510(k) number K872090.

Who is the listed applicant for THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT?

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 THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT?

The FDA product code for THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT is DQT.

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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: DQT)

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.

K983927GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORTArterial Vascular Engineering, Inc.K945963THE OMNIGUIDE GUIDING CATHETER WITH BALLOONMicro Interventional Systems, Inc.K910916CATHLAB SILICONE OCCLUSION BALLOON CATHETERCathlab Corp.K910339AVD INTIMAX OCCLUSION CATHETERApplied Vascular Devices, Inc.K880860CORONARY OSTIUM OCCLUDER, CATALOG CODE 32015Dlp, Inc.K880231MODIFIED PRUITT IRRIGATION & OCCLUSION CATHETERIdeas For Medicine, 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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