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FDA 510(k)

MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI

K-Number: K932375 · 1993-09-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1993-09-07
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K932375. 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 MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI?

MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K932375.

When did MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI receive FDA 510(k) clearance?

MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI received FDA 510(k) clearance on 1993-09-07, under 510(k) number K932375.

Who is the listed applicant for MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI?

The FDA product code for MAG RES DIAG DEV ACCESS CIR POL(CP) BODY/SPINE COI is LNH.

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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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