FlowMet
K-Number: K192966 · 2020-01-10
Device Summary
Frequently Asked Questions
What is the FlowMet?
FlowMet is a medical device that received FDA 510(k) clearance on 2020-01-10. The listed applicant is Laser Associated Sciences, Inc.. The 510(k) number is K192966.
When did FlowMet receive FDA 510(k) clearance?
FlowMet received FDA 510(k) clearance on 2020-01-10, under 510(k) number K192966.
Who is the listed applicant for FlowMet?
The FDA 510(k) record lists Laser Associated Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FlowMet?
The FDA product code for FlowMet is DPW.
Other records listing Laser Associated Sciences, 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.
Related Devices (Code: DPW)
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.