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FDA 510(k)

EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION

K-Number: K000237 · 2000-06-13

Decision Date2000-06-13
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION is the device name listed in this FDA 510(k) record. The listed applicant is Cybercare, Inc.. It received FDA 510(k) clearance on 2000-06-13 under 510(k) number K000237. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION?

EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION is a medical device that received FDA 510(k) clearance on 2000-06-13. The listed applicant is Cybercare, Inc.. The 510(k) number is K000237.

When did EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION receive FDA 510(k) clearance?

EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION received FDA 510(k) clearance on 2000-06-13, under 510(k) number K000237.

Who is the listed applicant for EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION?

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

What is the FDA product code for EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION?

The FDA product code for EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION is DXN.

Related Clinical Trials

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.

Other records listing Cybercare, Inc. 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.

Related Devices (Code: DXN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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