510(k) K963526

STRAP WEDGE by Alimed, Inc. — Product Code FMQ

K963526 is an FDA 510(k) premarket notification submitted by Alimed, Inc. for the device "STRAP WEDGE". The FDA issued a decision of Substantially Equivalent on October 28, 1996. The device falls under product code FMQ (Restraint, Protective), a Class I device regulated under 21 CFR 880.6760. Alimed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 28, 1996
Date Received
September 4, 1996
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