POWER 5000 GENERAL PURPOSE COIL
K-Number: K002483 · 2000-10-25
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Device Summary
Frequently Asked Questions
What is the POWER 5000 GENERAL PURPOSE COIL?
POWER 5000 GENERAL PURPOSE COIL is a medical device that received FDA 510(k) clearance on 2000-10-25. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K002483.
When did POWER 5000 GENERAL PURPOSE COIL receive FDA 510(k) clearance?
POWER 5000 GENERAL PURPOSE COIL received FDA 510(k) clearance on 2000-10-25, under 510(k) number K002483.
Who is the listed applicant for POWER 5000 GENERAL PURPOSE 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 POWER 5000 GENERAL PURPOSE COIL?
The FDA product code for POWER 5000 GENERAL PURPOSE 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.
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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