FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT

K Number: K844976 · Decision Apr 1, 1985
Classifications
1
FEI Numbers
206
Registration Numbers
207
Same Product Code
12
Applicant Total
4
Review Days
96

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Basic Information

Device Name
MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT
K Number
K844976
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5510
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Medi-Man Rehabilitation Products, Inc.
Date Received
December 26, 1984
Decision Date
April 1, 1985
Product Code
FSA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FSA Lift, Patient, Non-Ac-Powered

Similar 510(k) Clearances

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Other Clearances by Medi-Man Rehabilitation Products, Inc.

K Number Device Name
K992779 A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM
K925195 MALIBU BATHING SYSTEM
K924905 MEDI-PLINTH