WHEELCHAIR PATIENT RESTRAINTS

Accessories, Wheelchair

DANEK MEDICAL, INC.

The following data is part of a premarket notification filed by Danek Medical, Inc. with the FDA for Wheelchair Patient Restraints.

Pre-market Notification Details

Device IDK823816
510k NumberK823816
Device Name:WHEELCHAIR PATIENT RESTRAINTS
ClassificationAccessories, Wheelchair
Applicant DANEK MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKNO  
CFR Regulation Number890.3910 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-12-17
Decision Date1983-01-14

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