MORRISON MEDICAL WRIST RESTRAINT

Restraint, Protective

MORRISON MEDICAL PRODUCTS

The following data is part of a premarket notification filed by Morrison Medical Products with the FDA for Morrison Medical Wrist Restraint.

Pre-market Notification Details

Device IDK963419
510k NumberK963419
Device Name:MORRISON MEDICAL WRIST RESTRAINT
ClassificationRestraint, Protective
Applicant MORRISON MEDICAL PRODUCTS 2000 HOLLISTER DR. Libertyville,  IL  60048
ContactJoseph S Tokarz
CorrespondentJoseph S Tokarz
MORRISON MEDICAL PRODUCTS 2000 HOLLISTER DR. Libertyville,  IL  60048
Product CodeFMQ  
CFR Regulation Number880.6760 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-08-30
Decision Date1996-10-31
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00647921011724 K963419 000

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