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

INTERMITTENT COMPRESSION SYSTEM MODEL 5000

K Number: K930526 · Decision Nov 18, 1993
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
16
Review Days
289

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Basic Information

Device Name
INTERMITTENT COMPRESSION SYSTEM MODEL 5000
K Number
K930526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Advanced Instruments, Inc.
Date Received
February 2, 1993
Decision Date
November 18, 1993
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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