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FDA 510(k)

LIGHT REFLECTION RHEOGRAPHY

K-Number: K852378 · 1985-06-20

ApplicantHemodynamics, Inc.
Decision Date1985-06-20
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIGHT REFLECTION RHEOGRAPHY is the device name listed in this FDA 510(k) record. The listed applicant is Hemodynamics, Inc.. It received FDA 510(k) clearance on 1985-06-20 under 510(k) number K852378. 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 LIGHT REFLECTION RHEOGRAPHY?

LIGHT REFLECTION RHEOGRAPHY is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Hemodynamics, Inc.. The 510(k) number is K852378.

When did LIGHT REFLECTION RHEOGRAPHY receive FDA 510(k) clearance?

LIGHT REFLECTION RHEOGRAPHY received FDA 510(k) clearance on 1985-06-20, under 510(k) number K852378.

Who is the listed applicant for LIGHT REFLECTION RHEOGRAPHY?

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

What is the FDA product code for LIGHT REFLECTION RHEOGRAPHY?

The FDA product code for LIGHT REFLECTION RHEOGRAPHY 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 Hemodynamics, 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.

K881164LEUNOMED RFB 5000

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

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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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