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

MODEL 1750 STANDING URINAL

K Number: K790663 · Decision Apr 24, 1979
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
16
Applicant Total
19
Review Days
18

Basic Information

Device Name
MODEL 1750 STANDING URINAL
K Number
K790663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1800
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
LIFE-TECH INSTRUMENTS, INC.
Date Received
April 6, 1979
Decision Date
April 24, 1979
Product Code
FFG
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
FFG Device, Urine Flow Rate Measuring, Non-Electrical, Disposable

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