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FDA 510(k)

CHAMPION 5000 PERIPHERAL VASCULAR COIL

K-Number: K023247 · 2002-12-23

Decision Date2002-12-23
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CHAMPION 5000 PERIPHERAL VASCULAR COIL is the device name listed in this FDA 510(k) record. The listed applicant is Usa Instruments, Inc.. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K023247. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHAMPION 5000 PERIPHERAL VASCULAR COIL?

CHAMPION 5000 PERIPHERAL VASCULAR COIL is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K023247.

When did CHAMPION 5000 PERIPHERAL VASCULAR COIL receive FDA 510(k) clearance?

CHAMPION 5000 PERIPHERAL VASCULAR COIL received FDA 510(k) clearance on 2002-12-23, under 510(k) number K023247.

Who is the listed applicant for CHAMPION 5000 PERIPHERAL VASCULAR COIL?

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

What is the FDA product code for CHAMPION 5000 PERIPHERAL VASCULAR COIL?

The FDA product code for CHAMPION 5000 PERIPHERAL VASCULAR COIL is MOS.

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 Usa Instruments, 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 64 devices →

Related Devices (Code: MOS)

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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