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FDA 510(k)

SIENET TELERADIOLOGY PRODUCT LINE

K-Number: K955394 · 1996-02-21

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-02-21
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIENET TELERADIOLOGY PRODUCT LINE 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 1996-02-21 under 510(k) number K955394. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIENET TELERADIOLOGY PRODUCT LINE?

SIENET TELERADIOLOGY PRODUCT LINE is a medical device that received FDA 510(k) clearance on 1996-02-21. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K955394.

When did SIENET TELERADIOLOGY PRODUCT LINE receive FDA 510(k) clearance?

SIENET TELERADIOLOGY PRODUCT LINE received FDA 510(k) clearance on 1996-02-21, under 510(k) number K955394.

Who is the listed applicant for SIENET TELERADIOLOGY PRODUCT LINE?

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 SIENET TELERADIOLOGY PRODUCT LINE?

The FDA product code for SIENET TELERADIOLOGY PRODUCT LINE is LMC.

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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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