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

CODE 17-ENDOSCOPE DEODORANT

K Number: K840208 · Decision Jul 19, 1984
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
57
Applicant Total
1
Review Days
182

Basic Information

Device Name
CODE 17-ENDOSCOPE DEODORANT
K Number
K840208
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
KNOX LABORATORIES
Date Received
January 19, 1984
Decision Date
July 19, 1984
Product Code
FEB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FEB Accessories, Cleaning, For Endoscope

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