510(k) K812483

SECURA BATH SEAT by Maddak, Inc. — Product Code ILS

K812483 is an FDA 510(k) premarket notification submitted by Maddak, Inc. for the device "SECURA BATH SEAT". The FDA issued a decision of Substantially Equivalent on September 14, 1981. The device falls under product code ILS (Adaptor, Hygiene), a Class I device regulated under 21 CFR 890.5050. Maddak, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1981
Date Received
August 31, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Adaptor, Hygiene
Device Class
Class I
Regulation Number
890.5050
Review Panel
PM
Submission Type