The following data is part of a premarket notification filed by Medi-man Rehabilitation Products, Inc. with the FDA for Medi-man Water Powered Bath Lift & Hydraulic Lift.
Device ID | K844976 |
510k Number | K844976 |
Device Name: | MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT |
Classification | Lift, Patient, Non-ac-powered |
Applicant | MEDI-MAN REHABILITATION PRODUCTS, INC. 1020 MEYERSIDE DR., UNIT #1 Mississauga, CA |
Contact | Gordan Clard |
Correspondent | Gordan Clard MEDI-MAN REHABILITATION PRODUCTS, INC. 1020 MEYERSIDE DR., UNIT #1 Mississauga, CA |
Product Code | FSA |
CFR Regulation Number | 880.5510 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-12-26 |
Decision Date | 1985-04-01 |