BATH TUB SEAT & BATH BOARD

Aid, Transfer

ORTHION CORP.

The following data is part of a premarket notification filed by Orthion Corp. with the FDA for Bath Tub Seat & Bath Board.

Pre-market Notification Details

Device IDK823153
510k NumberK823153
Device Name:BATH TUB SEAT & BATH BOARD
ClassificationAid, Transfer
Applicant ORTHION CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIKX  
CFR Regulation Number890.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-10-20
Decision Date1982-11-05

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