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FDA 510(k)

FlowMet

K-Number: K192966 · 2020-01-10

ApplicantLaser Associated Sciences, Inc.
Decision Date2020-01-10
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FlowMet is a medical device manufactured by Laser Associated Sciences, Inc.. It received FDA 510(k) clearance on 2020-01-10 under approval number K192966. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FlowMet?

FlowMet is a medical device that received FDA 510(k) clearance on 2020-01-10. It is manufactured by Laser Associated Sciences, Inc.. The 510(k) number is K192966.

When was FlowMet approved by the FDA?

FlowMet received FDA 510(k) clearance on 2020-01-10, under approval number K192966.

What company makes FlowMet?

FlowMet is manufactured by Laser Associated Sciences, Inc..

What is the FDA product code for FlowMet?

The FDA product code for FlowMet is DPW.

Other Devices by Laser Associated Sciences, Inc.

K182494FlowMet-R

Related Devices (Code: DPW)

K152930PeriFlux6000Perimed AB K181269iCertaintyRfpi K172457Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDMDeltex Medical Limited K183574SRX Handheld Doppler, DMX Handheld Doppler, Obstetric Probes, Vascular ProbesHuntleigh Healthcare , Ltd. K191388FloPatch (FP110)Flosonics Medical (R/A 1929803 Ontario Corp.) K182494FlowMet-RLaser Associated Sciences, 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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