510(k) K962832

HEELBO QUILTED LIMB HOLDER WITH DOUBLE D-RING AND STRAP by Heelbo, Inc. — Product Code FMQ

K962832 is an FDA 510(k) premarket notification submitted by Heelbo, Inc. for the device "HEELBO QUILTED LIMB HOLDER WITH DOUBLE D-RING AND STRAP". The FDA issued a decision of Substantially Equivalent on October 18, 1996. The device falls under product code FMQ (Restraint, Protective), a Class I device regulated under 21 CFR 880.6760. Heelbo, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 18, 1996
Date Received
July 22, 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