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FDA 510(k)

MODIFIED BODY HELMHOLTZ COIL

K-Number: K930811 · 1993-09-07

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

Device Summary

MODIFIED BODY HELMHOLTZ COIL 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 K930811. 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 MODIFIED BODY HELMHOLTZ COIL?

MODIFIED BODY HELMHOLTZ COIL 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 K930811.

When did MODIFIED BODY HELMHOLTZ COIL receive FDA 510(k) clearance?

MODIFIED BODY HELMHOLTZ COIL received FDA 510(k) clearance on 1993-09-07, under 510(k) number K930811.

Who is the listed applicant for MODIFIED BODY HELMHOLTZ COIL?

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 MODIFIED BODY HELMHOLTZ COIL?

The FDA product code for MODIFIED BODY HELMHOLTZ COIL 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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