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

Arcadia Balloon Catheter

K Number: K191596 · Decision Oct 9, 2019
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
178
Review Days
114

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Basic Information

Device Name
Arcadia Balloon Catheter
K Number
K191596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Merit Medical Systems, Inc.
Date Received
June 17, 2019
Decision Date
October 9, 2019
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

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