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FDA 510(k)

CHEST FLUID MONITOR

K-Number: K772092 · 1977-11-18

ApplicantDynatech Research & Development Co.
Decision Date1977-11-18
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHEST FLUID MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Research & Development Co.. It received FDA 510(k) clearance on 1977-11-18 under 510(k) number K772092. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEST FLUID MONITOR?

CHEST FLUID MONITOR is a medical device that received FDA 510(k) clearance on 1977-11-18. The listed applicant is Dynatech Research & Development Co.. The 510(k) number is K772092.

When did CHEST FLUID MONITOR receive FDA 510(k) clearance?

CHEST FLUID MONITOR received FDA 510(k) clearance on 1977-11-18, under 510(k) number K772092.

Who is the listed applicant for CHEST FLUID MONITOR?

The FDA 510(k) record lists Dynatech Research & Development Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHEST FLUID MONITOR?

The FDA product code for CHEST FLUID MONITOR is DSB.

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.

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Other records listing Dynatech Research & Development Co. 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.

K772093IMPEDANCE RHEOGRAPH

Related Devices (Code: DSB)

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.

K260224MySOZO Software version 6.1.0.1 (SW version 6.1.0.1)ImpediMed LimitedK250634BCM2-Body Composition MonitorFresenius Medical Care Renal Therapies Group, LLCK243727Re:BalansMode Sensors ASK250922Edema Guard Monitor (EGM) CardioSet-001Cardioset Medical , Ltd.K232089SOZO ProImpediMed LimitedK223217Zynex Monitoring System, Model CM-1600Zynex Medical, Inc.

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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