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FDA 510(k)

MICROPLEX COIL SYSTEM-COSMOS

K-Number: K090891 · 2009-06-22

Decision Date2009-06-22
Product CodeHCG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICROPLEX COIL SYSTEM-COSMOS is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2009-06-22 under 510(k) number K090891. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPLEX COIL SYSTEM-COSMOS?

MICROPLEX COIL SYSTEM-COSMOS is a medical device that received FDA 510(k) clearance on 2009-06-22. The listed applicant is MicroVention, Inc.. The 510(k) number is K090891.

When did MICROPLEX COIL SYSTEM-COSMOS receive FDA 510(k) clearance?

MICROPLEX COIL SYSTEM-COSMOS received FDA 510(k) clearance on 2009-06-22, under 510(k) number K090891.

Who is the listed applicant for MICROPLEX COIL SYSTEM-COSMOS?

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 MICROPLEX COIL SYSTEM-COSMOS?

The FDA product code for MICROPLEX COIL SYSTEM-COSMOS is HCG.

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: HCG)

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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