VISION 9000 PHASED ARRAY TORSO COIL
K-Number: K002482 · 2000-10-17
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Device Summary
Frequently Asked Questions
What is the VISION 9000 PHASED ARRAY TORSO COIL?
VISION 9000 PHASED ARRAY TORSO COIL is a medical device that received FDA 510(k) clearance on 2000-10-17. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K002482.
When did VISION 9000 PHASED ARRAY TORSO COIL receive FDA 510(k) clearance?
VISION 9000 PHASED ARRAY TORSO COIL received FDA 510(k) clearance on 2000-10-17, under 510(k) number K002482.
Who is the listed applicant for VISION 9000 PHASED ARRAY TORSO 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 VISION 9000 PHASED ARRAY TORSO COIL?
The FDA product code for VISION 9000 PHASED ARRAY TORSO 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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