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510(k) K922550

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) by Verimed Holdings, Inc. — Product Code KQX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 10, 1992
Date Received
May 29, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Goniometer, Ac-Powered
Device Class
Class I
Regulation Number
888.1500
Review Panel
NE
Submission Type

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