510(k) K813641

VITAL METRICS URINE MONITORING SYSTEM by Vital Metrics, Inc. — Product Code FFG

K813641 is an FDA 510(k) premarket notification submitted by Vital Metrics, Inc. for the device "VITAL METRICS URINE MONITORING SYSTEM". The FDA issued a decision of Substantially Equivalent on March 1, 1982. The device falls under product code FFG (Device, Urine Flow Rate Measuring, Non-Electrical, Disposable), a Class II device regulated under 21 CFR 876.1800. Vital Metrics, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 1, 1982
Date Received
December 30, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Urine Flow Rate Measuring, Non-Electrical, Disposable
Device Class
Class II
Regulation Number
876.1800
Review Panel
GU
Submission Type