510(k) K922550

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

K922550 is an FDA 510(k) premarket notification submitted by Verimed Holdings, Inc. for the device "ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)". The FDA issued a decision of Substantially Equivalent on December 10, 1992. The device falls under product code KQX (Goniometer, Ac-Powered), a Class I device regulated under 21 CFR 888.1500. Verimed Holdings, Inc. has at least 10 other 510(k) clearances on record.

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