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

VITAL METRICS URINE MONITORING SYSTEM

K Number: K813641 · Decision Mar 1, 1982
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
16
Applicant Total
9
Review Days
61

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Basic Information

Device Name
VITAL METRICS URINE MONITORING SYSTEM
K Number
K813641
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1800
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Vital Metrics, Inc.
Date Received
December 30, 1981
Decision Date
March 1, 1982
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FFG), ordered by most recent decision date.

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Other Clearances by Vital Metrics, Inc.

K Number Device Name
K883201 VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS
K882956 VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION
K844973 IRRIGA SUC ILLUM ISIS 710 & 7100 SERIES
K843441 URINARY DRAINAGE CONTAINER 2012-WITH
K843442 URINARY DRAINAGE CONTAINER 2013 WITH
K840917 URINARY MONITORING SYS 240
K834448 URINARY DRAINAGE CONTAINER
K832526 UROTRACK PLUS