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FDA 510(k)

IMPEDANCE RHEOGRAPH

K-Number: K772093 · 1977-11-18

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

Device Summary

IMPEDANCE RHEOGRAPH 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 K772093. The device is classified under product code DQB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPEDANCE RHEOGRAPH?

IMPEDANCE RHEOGRAPH 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 K772093.

When did IMPEDANCE RHEOGRAPH receive FDA 510(k) clearance?

IMPEDANCE RHEOGRAPH received FDA 510(k) clearance on 1977-11-18, under 510(k) number K772093.

Who is the listed applicant for IMPEDANCE RHEOGRAPH?

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 IMPEDANCE RHEOGRAPH?

The FDA product code for IMPEDANCE RHEOGRAPH is DQB.

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.

K772092CHEST FLUID MONITOR

Related Devices (Code: DQB)

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.

K851102VASOSCREEN IMPEDANCE PLETHYSMOGRAPHSonicaid, Inc.K822873DEVETHERMEko Scann AB

Official Source

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

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