Heelbo Quilted Torso Restraint

FDA 510(k) K963108 · Hollister, Inc.

Substantially Equivalent

510(k) numberK963108

Submission

Device name
Heelbo Quilted Torso Restraint
Applicant
Hollister, Inc.
Libertyville, IL, US
Received
August 12, 1996
Decision date
October 9, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMQ – Restraint, Protective
Device class
Class I (low risk)
Regulation
21 CFR 880.6760
Specialty
General Hospital

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Questions and answers

When was Heelbo Quilted Torso Restraint cleared by the FDA?

Heelbo Quilted Torso Restraint (K963108) received a 510(k) decision of Substantially Equivalent on October 9, 1996, 58 days after the submission was received.

What is the product code of K963108?

The FDA product code is FMQ – Restraint, Protective, a Class I (low risk) device regulated under 21 CFR 880.6760.