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

DELIVERY SHEATH, MODEL ADELANTE BREEZEWAY

K Number: K122958 · Decision Dec 13, 2012
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
49
Review Days
79

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Basic Information

Device Name
DELIVERY SHEATH, MODEL ADELANTE BREEZEWAY
K Number
K122958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oscor, Inc.
Date Received
September 25, 2012
Decision Date
December 13, 2012
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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Other Clearances by Oscor, Inc.

K Number Device Name
K210627 Breezeway II
K151951 Destino Reach
K143463 IS4/DF4 Port Plug
K140917 INTRODUCER, MODEL ADELANTE MAGNUM
K140406 DESTINO TWIST, STEERABLE GUIDING SHEATH
K130633 INTRODUCER SETS, MODEL ADELANTE RADIAL
K130843 SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE
K130104 GUIDEWIRE, PURSUER SERIES
K122960 STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO
K122084 INTRODUCER SET, MODEL ADELANTE-S SERIES
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