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

TALLEY MICRO SYSTEM/TALLEY RIPPLEBED

K Number: K914775 · Decision Apr 10, 1992
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
101
Applicant Total
6
Review Days
170

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Basic Information

Device Name
TALLEY MICRO SYSTEM/TALLEY RIPPLEBED
K Number
K914775
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5550
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Talley Group, Ltd.
Date Received
October 23, 1991
Decision Date
April 10, 1992
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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K Number Device Name
K151263 Venturi Gauze Wound Care Sets with Portal Drain
K143004 VENTURI MiNO TG600/14
K914774 MULTIPULSE SEQUENTIAL COMPRESSION UNIT
K914780 TALLEY SD.500 SKIN PRESSURE EVALUATOR
K914776 OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITOR