FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

CARECOMPANION PATIENT STATION & NURSE STATION

K Number: K022274 · Decision May 29, 2003
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
190
Applicant Total
4
Review Days
318

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Basic Information

Device Name
CARECOMPANION PATIENT STATION & NURSE STATION
K Number
K022274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2910
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neptec Design Group, Ltd.
Date Received
July 15, 2002
Decision Date
May 29, 2003
Product Code
DRG
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DRG), ordered by most recent decision date.

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Other Clearances by Neptec Design Group, Ltd.

K Number Device Name
K023286 CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION
K020584 N2000 BASE STATION; N2001 NURSE STATION
K012801 N2000 BASE STATION, N2001 NURSE STATION