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

COMPACTCATH INTERMITTENT URINARY CATHETER

K Number: K140945 · Decision Aug 22, 2014
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
81
Applicant Total
3
Review Days
130

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Basic Information

Device Name
COMPACTCATH INTERMITTENT URINARY CATHETER
K Number
K140945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Compactcath, Inc.
Date Received
April 14, 2014
Decision Date
August 22, 2014
Product Code
EZD
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EZD Catheter, Straight

Similar 510(k) Clearances

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

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Other Clearances by Compactcath, Inc.

K Number Device Name
K180738 COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter
K160858 CompactCath Intermittent Urinary Catheter