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FDA 510(k)

VAGABOND SOFT RESTRAINT SYSTEM

K-Number: K982178 · 1999-01-26

ApplicantEmergent Innovations, Ltd.
Decision Date1999-01-26
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAGABOND SOFT RESTRAINT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Emergent Innovations, Ltd.. It received FDA 510(k) clearance on 1999-01-26 under 510(k) number K982178. 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 VAGABOND SOFT RESTRAINT SYSTEM?

VAGABOND SOFT RESTRAINT SYSTEM is a medical device that received FDA 510(k) clearance on 1999-01-26. The listed applicant is Emergent Innovations, Ltd.. The 510(k) number is K982178.

When did VAGABOND SOFT RESTRAINT SYSTEM receive FDA 510(k) clearance?

VAGABOND SOFT RESTRAINT SYSTEM received FDA 510(k) clearance on 1999-01-26, under 510(k) number K982178.

Who is the listed applicant for VAGABOND SOFT RESTRAINT SYSTEM?

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

What is the FDA product code for VAGABOND SOFT RESTRAINT SYSTEM?

The FDA product code for VAGABOND SOFT RESTRAINT SYSTEM 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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