FDA 510(k)

INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL

K-Number: K023650 · 2003-01-24

Decision Date2003-01-24

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS 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 2003-01-24 under 510(k) number K023650. 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 INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL?

INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL is a medical device that received FDA 510(k) clearance on 2003-01-24. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K023650.

When did INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL receive FDA 510(k) clearance?

INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL received FDA 510(k) clearance on 2003-01-24, under 510(k) number K023650.

Who is the listed applicant for INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS 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 INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL?

The FDA product code for INSIGHT PLUS 9000 PHASED ARRAY TORSO AND PLEVIS COIL is MOS.

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Related Devices (Code: MOS)

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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.