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FDA 510(k)

VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE

K-Number: K961716 · 1996-09-19

Decision Date1996-09-19
Product CodeDXE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE 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 1996-09-19 under 510(k) number K961716. The device is classified under product code DXE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE?

VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE is a medical device that received FDA 510(k) clearance on 1996-09-19. The listed applicant is Ideas For Medicine, Inc.. The 510(k) number is K961716.

When did VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE receive FDA 510(k) clearance?

VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE received FDA 510(k) clearance on 1996-09-19, under 510(k) number K961716.

Who is the listed applicant for VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE?

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 VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE?

The FDA product code for VASO-SAFE ARTERIAL EMBOLECTOMY CATHETE is DXE.

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.

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.

View all 15 devices →

Related Devices (Code: DXE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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