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FDA 510(k)

HYDROCOIL EMBOLIC SYSTEMS (HES)

K-Number: K071939 · 2008-01-11

Decision Date2008-01-11
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HYDROCOIL EMBOLIC SYSTEMS (HES) is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2008-01-11 under 510(k) number K071939. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDROCOIL EMBOLIC SYSTEMS (HES)?

HYDROCOIL EMBOLIC SYSTEMS (HES) is a medical device that received FDA 510(k) clearance on 2008-01-11. The listed applicant is MicroVention, Inc.. The 510(k) number is K071939.

When did HYDROCOIL EMBOLIC SYSTEMS (HES) receive FDA 510(k) clearance?

HYDROCOIL EMBOLIC SYSTEMS (HES) received FDA 510(k) clearance on 2008-01-11, under 510(k) number K071939.

Who is the listed applicant for HYDROCOIL EMBOLIC SYSTEMS (HES)?

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

What is the FDA product code for HYDROCOIL EMBOLIC SYSTEMS (HES)?

The FDA product code for HYDROCOIL EMBOLIC SYSTEMS (HES) is KRD.

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 MicroVention, 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 77 devices →

Related Devices (Code: KRD)

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

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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