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FDA 510(k)

HEELBO QUILTED TORSO RESTRAINT

K-Number: K963108 · 1996-10-09

ApplicantHollister, Inc.
Decision Date1996-10-09
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEELBO QUILTED TORSO RESTRAINT is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1996-10-09 under 510(k) number K963108. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEELBO QUILTED TORSO RESTRAINT?

HEELBO QUILTED TORSO RESTRAINT is a medical device that received FDA 510(k) clearance on 1996-10-09. The listed applicant is Hollister, Inc.. The 510(k) number is K963108.

When did HEELBO QUILTED TORSO RESTRAINT receive FDA 510(k) clearance?

HEELBO QUILTED TORSO RESTRAINT received FDA 510(k) clearance on 1996-10-09, under 510(k) number K963108.

Who is the listed applicant for HEELBO QUILTED TORSO RESTRAINT?

The FDA 510(k) record lists Hollister, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEELBO QUILTED TORSO RESTRAINT?

The FDA product code for HEELBO QUILTED TORSO RESTRAINT is FMQ.

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Related Devices (Code: FMQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K110377PROTECTIVE RESTRAINTMedi-Tech Intl. Corp.K081264STATSTRAP NEONATAL INCUBATOR SAFETY STRAP, MODELS SS-001, SS-002Children'S Health First, Inc.K080448CENTURION PROTECTIVE RESTRAINT, SCR SERIESTri-State Hospital Supply Corp.K013239COMFORTCARE COMPRESSION SUPPORT WITH MAGNETS COMFORTCARE MAGNETIC INSOLESMed Gen, Inc.K010818INFANT LIMB HOLDER, MODELS 306080 & 306081Skil-Care Corp.K010644CINCH-TYPE DISPOSABLE LIMB HOLDERS, MODEL 912025Skil-Care Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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