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

SoloPath Re-Collapsible Access System

K Number: K152498 · Decision Jan 5, 2016
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
8
Review Days
126

Basic Information

Device Name
SoloPath Re-Collapsible Access System
K Number
K152498
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ONSET MEDICAL CORPORATION
Date Received
September 1, 2015
Decision Date
January 5, 2016
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYB), ordered by most recent decision date.

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Other Clearances by ONSET MEDICAL CORPORATION

K Number Device Name
K121404 SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM
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K092014 SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER
K062852 BALLOON EXPANDABLE TRANSSEPTAL INDRODUCER, MODELS BETI-1840 AND BETI-1870
K061009 PATHWAY BALLOON EXPANDABLE URETERAL ACCESS SHEATH, MODEL BEUS
K043254 PATHWAY URETERAL ACCESS SHEATH, PATHWAY EXPANDABLE URETERAL ACCESS SHEATH