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

LAVAGING CATHETERS

K Number: K822061 · Decision Jul 20, 1982
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
90
Applicant Total
19
Review Days
7

Basic Information

Device Name
LAVAGING CATHETERS
K Number
K822061
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
AMERICAN ENDOSCOPY, INC.
Date Received
July 13, 1982
Decision Date
July 20, 1982
Product Code
OCX
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
OCX Endoscopic Irrigation/Suction System

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K833492 PERCUTANEOUS ENDOSCOPIC GASTROSCOPY
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