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FDA 510(k)

STUCKEY STRAP-3 FINGER RESTRAINTS

K-Number: K963491 · 1996-11-14

ApplicantStuckey Ent., Inc.
Decision Date1996-11-14
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STUCKEY STRAP-3 FINGER RESTRAINTS is the device name listed in this FDA 510(k) record. The listed applicant is Stuckey Ent., Inc.. It received FDA 510(k) clearance on 1996-11-14 under 510(k) number K963491. 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 STUCKEY STRAP-3 FINGER RESTRAINTS?

STUCKEY STRAP-3 FINGER RESTRAINTS is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Stuckey Ent., Inc.. The 510(k) number is K963491.

When did STUCKEY STRAP-3 FINGER RESTRAINTS receive FDA 510(k) clearance?

STUCKEY STRAP-3 FINGER RESTRAINTS received FDA 510(k) clearance on 1996-11-14, under 510(k) number K963491.

Who is the listed applicant for STUCKEY STRAP-3 FINGER RESTRAINTS?

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

What is the FDA product code for STUCKEY STRAP-3 FINGER RESTRAINTS?

The FDA product code for STUCKEY STRAP-3 FINGER RESTRAINTS 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

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

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