FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WATER FLOATION BED 800/TC/H

K Number: K840881 · Decision Jul 18, 1984
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
56
Applicant Total
4
Review Days
142

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
WATER FLOATION BED 800/TC/H
K Number
K840881
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5170
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Western Medical, Ltd.
Date Received
February 27, 1984
Decision Date
July 18, 1984
Product Code
IOQ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IOQ Bed, Flotation Therapy, Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IOQ), ordered by most recent decision date.

View all

Other Clearances by Western Medical, Ltd.

K Number Device Name
K894387 WESTCO MADAYAG PAB NEEDLE
K891459 STERILE BURNNET PRE-CUT (VARIOUS SIZES)
K840882 HOME CARE WATER FLOTATION BED HC4/TC/H