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FDA 510(k)

CLINICAL PROTON SPECTROSCOPY OPTION

K-Number: K951650 · 1995-11-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-11-14
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLINICAL PROTON SPECTROSCOPY OPTION 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 1995-11-14 under 510(k) number K951650. 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 CLINICAL PROTON SPECTROSCOPY OPTION?

CLINICAL PROTON SPECTROSCOPY OPTION is a medical device that received FDA 510(k) clearance on 1995-11-14. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K951650.

When did CLINICAL PROTON SPECTROSCOPY OPTION receive FDA 510(k) clearance?

CLINICAL PROTON SPECTROSCOPY OPTION received FDA 510(k) clearance on 1995-11-14, under 510(k) number K951650.

Who is the listed applicant for CLINICAL PROTON SPECTROSCOPY OPTION?

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 CLINICAL PROTON SPECTROSCOPY OPTION?

The FDA product code for CLINICAL PROTON SPECTROSCOPY OPTION is LNH.

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Official Source

View on FDA Database →

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