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FDA 510(k)

EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION

K-Number: K003257 · 2000-12-22

Decision Date2000-12-22
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION is the device name listed in this FDA 510(k) record. The listed applicant is Cybercare Technologies, Inc.. It received FDA 510(k) clearance on 2000-12-22 under 510(k) number K003257. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION?

EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION is a medical device that received FDA 510(k) clearance on 2000-12-22. The listed applicant is Cybercare Technologies, Inc.. The 510(k) number is K003257.

When did EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION receive FDA 510(k) clearance?

EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION received FDA 510(k) clearance on 2000-12-22, under 510(k) number K003257.

Who is the listed applicant for EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION?

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

What is the FDA product code for EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION?

The FDA product code for EHC400 DESKTOP PATIENT STATION; ECH600 CARE PROVIDER STATION is CGA.

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 Technologies, 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: CGA)

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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