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

SPR PLUS II OVERLAY SYSTEM (CL250/CL212

K Number: K961854 · Decision Aug 9, 1996
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
101
Applicant Total
27
Review Days
87

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Basic Information

Device Name
SPR PLUS II OVERLAY SYSTEM (CL250/CL212
K Number
K961854
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5550
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gaymar Industries, Inc.
Date Received
May 14, 1996
Decision Date
August 9, 1996
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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K963067 SOF. PRESS EPC 51 SYSTEM
K942881 TC 3000
K930345 TC2000 POWER UNIT AND ACCESSORIES
K914921 SCM-3 AND ACCESSORIES
K914805 TC-1000, TC-1050 SYSTEM
K914851 CLA-1400 SYSTEM
K912051 MEDI-THERM (MTA-5900) & DETACHABLE HOSES
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