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

TURBO II

K Number: K933402 · Decision Mar 15, 1994
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
101
Applicant Total
48
Review Days
246

Basic Information

Device Name
TURBO II
K Number
K933402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5550
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
KINETIC CONCEPTS, INC.
Date Received
July 12, 1993
Decision Date
March 15, 1994
Product Code
FNM
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
FNM Mattress, Air Flotation, Alternating Pressure

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