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

SOF. PRESS EPC 51 SYSTEM

K Number: K963067 · Decision Jan 28, 1997
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
27
Review Days
174

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Basic Information

Device Name
SOF. PRESS EPC 51 SYSTEM
K Number
K963067
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gaymar Industries, Inc.
Date Received
August 7, 1996
Decision Date
January 28, 1997
Product Code
JOW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
JOW Sleeve, Limb, Compressible

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K961854 SPR PLUS II OVERLAY SYSTEM (CL250/CL212
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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