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FDA 510(k)

PRIMA III TOTALSENSE TORSO COIL

K-Number: K030371 · 2003-05-05

Decision Date2003-05-05
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRIMA III TOTALSENSE TORSO 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 2003-05-05 under 510(k) number K030371. 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 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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