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Medi-Man Rehabilitation Products, Inc.

FDA Regulatory Profile

Medi-Man Rehabilitation Products, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 13, 2000.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992779A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEMJanuary 13, 2000
K925195MALIBU BATHING SYSTEMOctober 17, 1994
K924905MEDI-PLINTHFebruary 16, 1993
K844976MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFTApril 1, 1985

FDA data resources