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

Radial Medical Compression System

K Number: K181651 · Decision Oct 12, 2018
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
2
Review Days
112

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Basic Information

Device Name
Radial Medical Compression System
K Number
K181651
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radial Medical, Inc.
Date Received
June 22, 2018
Decision Date
October 12, 2018
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

Similar 510(k) Clearances

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Other Clearances by Radial Medical, Inc.

K Number Device Name
K190976 Radial Medical Compression System