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FDA 510(k)

SIENET DICOM GATEWAY

K-Number: K952533 · 1995-08-23

ApplicantSiemens AG
Decision Date1995-08-23
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIENET DICOM GATEWAY is the device name listed in this FDA 510(k) record. The listed applicant is Siemens AG. It received FDA 510(k) clearance on 1995-08-23 under 510(k) number K952533. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIENET DICOM GATEWAY?

SIENET DICOM GATEWAY is a medical device that received FDA 510(k) clearance on 1995-08-23. The listed applicant is Siemens AG. The 510(k) number is K952533.

When did SIENET DICOM GATEWAY receive FDA 510(k) clearance?

SIENET DICOM GATEWAY received FDA 510(k) clearance on 1995-08-23, under 510(k) number K952533.

Who is the listed applicant for SIENET DICOM GATEWAY?

The FDA 510(k) record lists Siemens AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIENET DICOM GATEWAY?

The FDA product code for SIENET DICOM GATEWAY is LMD.

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Other records listing Siemens AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123375SYNGO.VIAK110366SYNGO.CT CARDIAC FUNCTIONK071310SYNGO CT ONCOLOGY SOFTWARE PACKAGEK063507SYNGO NEURO PBV CTK063373FLEX LOOP COIL SET 3TK053024SYNGO NEURO DSA CT

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Related Devices (Code: LMD)

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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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