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510(k) K914859

BARTRONIX IN-BED ACTIVITY MONITOR by Bartronix — Product Code KMI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 13, 1992
Date Received
October 29, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Bed Patient
Device Class
Class I
Regulation Number
880.2400
Review Panel
HO
Submission Type

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