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FDA 510(k)

VITAL METRICS URINE MONITORING SYSTEM

K-Number: K813641 · 1982-03-01

Decision Date1982-03-01
Product CodeFFG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VITAL METRICS URINE MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vital Metrics, Inc.. It received FDA 510(k) clearance on 1982-03-01 under 510(k) number K813641. The device is classified under product code FFG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL METRICS URINE MONITORING SYSTEM?

VITAL METRICS URINE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is Vital Metrics, Inc.. The 510(k) number is K813641.

When did VITAL METRICS URINE MONITORING SYSTEM receive FDA 510(k) clearance?

VITAL METRICS URINE MONITORING SYSTEM received FDA 510(k) clearance on 1982-03-01, under 510(k) number K813641.

Who is the listed applicant for VITAL METRICS URINE MONITORING SYSTEM?

The FDA 510(k) record lists Vital Metrics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAL METRICS URINE MONITORING SYSTEM?

The FDA product code for VITAL METRICS URINE MONITORING SYSTEM is FFG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Vital Metrics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: FFG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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