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FDA 510(k)

9750 ATHENA ETHERNET OPTION

K-Number: K934887 · 1994-01-14

ApplicantS & W Medico Teknik A/S
Decision Date1994-01-14
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

9750 ATHENA ETHERNET OPTION is the device name listed in this FDA 510(k) record. The listed applicant is S & W Medico Teknik A/S. It received FDA 510(k) clearance on 1994-01-14 under 510(k) number K934887. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 9750 ATHENA ETHERNET OPTION?

9750 ATHENA ETHERNET OPTION is a medical device that received FDA 510(k) clearance on 1994-01-14. The listed applicant is S & W Medico Teknik A/S. The 510(k) number is K934887.

When did 9750 ATHENA ETHERNET OPTION receive FDA 510(k) clearance?

9750 ATHENA ETHERNET OPTION received FDA 510(k) clearance on 1994-01-14, under 510(k) number K934887.

Who is the listed applicant for 9750 ATHENA ETHERNET OPTION?

The FDA 510(k) record lists S & W Medico Teknik A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 9750 ATHENA ETHERNET OPTION?

The FDA product code for 9750 ATHENA ETHERNET OPTION is DXK.

Related Clinical Trials

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Other records listing S & W Medico Teknik A/S 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.

K964593DIASCOPE TRAVELLER PLUS (4053)K9421963050 DIASCOPE NT PATIENT MONITOR

Related Devices (Code: DXK)

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.

K181042Ultra ICE Plus – PI 9 MHz Peripheral Imaging CatheterBoston Scientific CorporationK160173Ultra ICE Plus 9 MHz IntraCardiac Echo Catheter(eDFU), Ultra ICE Plus 9 MHz IntraCardiac Echo Catheter (Paper DFU)Boston Scientific CorporationK031148IN-VISION IMAGING SYSTEMJomed, Inc.K913209ACCESSORY TO GENESIS III (GCFM)Biosound, Inc.K911384CATHSCANNER(R) VISIONS(TM) 3.5F 54700/5.0F 54600Endosonics Corp.K904832MODIFIED SYST: SONOS 500/1000 ULTRSOUND IMAG SYSTHewlett-Packard Co.

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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