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

UROLOGICAL GUIDWIRE

K Number: K944135 · Decision Sep 21, 1994
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
63
Applicant Total
58
Review Days
28

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Basic Information

Device Name
UROLOGICAL GUIDWIRE
K Number
K944135
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Applied Medical Resources
Date Received
August 24, 1994
Decision Date
September 21, 1994
Product Code
KNY
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
KNY Accessories, Catheter, G-U

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