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

MANAN VS ACCESS NEEDLE/SET

K Number: K980372 · Decision Apr 27, 1998
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
464
Applicant Total
46
Review Days
87

Basic Information

Device Name
MANAN VS ACCESS NEEDLE/SET
K Number
K980372
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDICAL DEVICE TECHNOLOGIES, INC.
Date Received
January 30, 1998
Decision Date
April 27, 1998
Product Code
FGE
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
FGE Stents, Drains And Dilators For The Biliary Ducts

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