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

MEDOVATIONS ESOPHAGEAL DILATOR

K Number: K002363 · Decision Nov 1, 2000
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
39
Applicant Total
31
Review Days
90

Basic Information

Device Name
MEDOVATIONS ESOPHAGEAL DILATOR
K Number
K002363
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5365
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDOVATIONS, INC.
Date Received
August 3, 2000
Decision Date
November 1, 2000
Product Code
KNQ
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
KNQ Dilator, Esophageal

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