PRIMA III TOTALSENSE TORSO COIL
K-Number: K030371 · 2003-05-05
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Device Summary
Frequently Asked Questions
What is the PRIMA III TOTALSENSE TORSO COIL?
PRIMA III TOTALSENSE TORSO COIL is a medical device that received FDA 510(k) clearance on 2003-05-05. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K030371.
When did PRIMA III TOTALSENSE TORSO COIL receive FDA 510(k) clearance?
PRIMA III TOTALSENSE TORSO COIL received FDA 510(k) clearance on 2003-05-05, under 510(k) number K030371.
Who is the listed applicant for PRIMA III TOTALSENSE 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 PRIMA III TOTALSENSE TORSO COIL?
The FDA product code for PRIMA III TOTALSENSE 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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