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

LOW AIR LOSS MATTRESS, MODIFICATION

K Number: K934689 · Decision Feb 2, 1994
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
27
Applicant Total
9
Review Days
163

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Basic Information

Device Name
LOW AIR LOSS MATTRESS, MODIFICATION
K Number
K934689
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5160
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cardio Systems, Inc.
Date Received
August 23, 1993
Decision Date
February 2, 1994
Product Code
INX
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
INX Bed, Air Fluidized

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