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

ARSTASIS ACCESS SYSTEM

K Number: K102728 · Decision Oct 7, 2010
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
14
Review Days
15

Basic Information

Device Name
ARSTASIS ACCESS SYSTEM
K Number
K102728
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ARSTASIS, INC.
Date Received
September 22, 2010
Decision Date
October 7, 2010
Product Code
DYB
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
DYB Introducer, Catheter

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K123618 AXERA 2 ACCESS SYSTEM
K123135 AXERA 2 ACCESS SYSTEM MODEL AXE200
K121521 AXERA ACCESS SYSTEM
K113110 AXERA ACCESS SYSTEM
K103421 ARSTASIS DILATOR ADAPTER
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