CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION
K-Number: K023286 · 2003-05-02
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Device Summary
Frequently Asked Questions
What is the CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION?
CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION is a medical device that received FDA 510(k) clearance on 2003-05-02. The listed applicant is Neptec Design Group, Ltd.. The 510(k) number is K023286.
When did CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION receive FDA 510(k) clearance?
CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION received FDA 510(k) clearance on 2003-05-02, under 510(k) number K023286.
Who is the listed applicant for CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION?
The FDA 510(k) record lists Neptec Design Group, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION?
The FDA product code for CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT 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 Neptec Design Group, Ltd. 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
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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