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FDA 510(k)

SUPERSENSOR MRI COIL

K-Number: K941582 · 1994-12-23

ApplicantSuperconductor Technologies, Inc.
Decision Date1994-12-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SUPERSENSOR MRI COIL is the device name listed in this FDA 510(k) record. The listed applicant is Superconductor Technologies, Inc.. It received FDA 510(k) clearance on 1994-12-23 under 510(k) number K941582. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERSENSOR MRI COIL?

SUPERSENSOR MRI COIL is a medical device that received FDA 510(k) clearance on 1994-12-23. The listed applicant is Superconductor Technologies, Inc.. The 510(k) number is K941582.

When did SUPERSENSOR MRI COIL receive FDA 510(k) clearance?

SUPERSENSOR MRI COIL received FDA 510(k) clearance on 1994-12-23, under 510(k) number K941582.

Who is the listed applicant for SUPERSENSOR MRI COIL?

The FDA 510(k) record lists Superconductor Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPERSENSOR MRI COIL?

The FDA product code for SUPERSENSOR MRI COIL is LNH.

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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.

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