HYDROCOIL EMBOLIC SYSTEMS (HES)
K-Number: K071939 · 2008-01-11
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Device Summary
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.
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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