510(k) K970275

PATIENT RESTRAINTS by Fla Orthopedics, Inc. — Product Code FMQ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 11, 1997
Date Received
January 23, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Restraint, Protective
Device Class
Class I
Regulation Number
880.6760
Review Panel
HO
Submission Type