MARK 5000 PHASED ARRAY SHOULDER COIL
K-Number: K983143 · 1998-11-16
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Device Summary
Frequently Asked Questions
What is the MARK 5000 PHASED ARRAY SHOULDER COIL?
MARK 5000 PHASED ARRAY SHOULDER COIL is a medical device that received FDA 510(k) clearance on 1998-11-16. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K983143.
When did MARK 5000 PHASED ARRAY SHOULDER COIL receive FDA 510(k) clearance?
MARK 5000 PHASED ARRAY SHOULDER COIL received FDA 510(k) clearance on 1998-11-16, under 510(k) number K983143.
Who is the listed applicant for MARK 5000 PHASED ARRAY SHOULDER 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 MARK 5000 PHASED ARRAY SHOULDER COIL?
The FDA product code for MARK 5000 PHASED ARRAY SHOULDER 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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