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FDA 510(k)

SIEMENS CLINICAL WORK STATION

K-Number: K935043 · 1995-04-07

ApplicantSiemens Medical Electronics
Decision Date1995-04-07
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS CLINICAL WORK STATION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1995-04-07 under 510(k) number K935043. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS CLINICAL WORK STATION?

SIEMENS CLINICAL WORK STATION is a medical device that received FDA 510(k) clearance on 1995-04-07. The listed applicant is Siemens Medical Electronics. The 510(k) number is K935043.

When did SIEMENS CLINICAL WORK STATION receive FDA 510(k) clearance?

SIEMENS CLINICAL WORK STATION received FDA 510(k) clearance on 1995-04-07, under 510(k) number K935043.

Who is the listed applicant for SIEMENS CLINICAL WORK STATION?

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

What is the FDA product code for SIEMENS CLINICAL WORK STATION?

The FDA product code for SIEMENS CLINICAL WORK STATION is DQK.

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Other records listing Siemens Medical Electronics 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.

K921930SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFIK920445SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIESK914765SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYSK912070SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNITK913489SIEMENS MICRO2 PULSE OXIMETERK905775SIEMENS ETCO2 CARTRIDGE

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Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

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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