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

ENEMA TUBE

K Number: K832501 · Decision Aug 31, 1983
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
4
Review Days
35

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Basic Information

Device Name
ENEMA TUBE
K Number
K832501
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Cone Instruments, Inc.
Date Received
July 27, 1983
Decision Date
August 31, 1983
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

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