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FDA 510(k)

CompuFlo Epidural Computer Controlled Anesthesia System

K-Number: K221702 · 2023-02-25

ApplicantMilestone Scientific, Inc.
Decision Date2023-02-25
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CompuFlo Epidural Computer Controlled Anesthesia System is a medical device manufactured by Milestone Scientific, Inc.. It received FDA 510(k) clearance on 2023-02-25 under approval number K221702. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CompuFlo Epidural Computer Controlled Anesthesia System?

CompuFlo Epidural Computer Controlled Anesthesia System is a medical device that received FDA 510(k) clearance on 2023-02-25. It is manufactured by Milestone Scientific, Inc.. The 510(k) number is K221702.

When was CompuFlo Epidural Computer Controlled Anesthesia System approved by the FDA?

CompuFlo Epidural Computer Controlled Anesthesia System received FDA 510(k) clearance on 2023-02-25, under approval number K221702.

What company makes CompuFlo Epidural Computer Controlled Anesthesia System?

CompuFlo Epidural Computer Controlled Anesthesia System is manufactured by Milestone Scientific, Inc..

What is the FDA product code for CompuFlo Epidural Computer Controlled Anesthesia System?

The FDA product code for CompuFlo Epidural Computer Controlled Anesthesia System is FMF.

Related Clinical Trials

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Related PubMed Literature

PMID: 41612341 Brain-computer interface commercialization. Journal of neuroengineering and rehabilitation (2026)

Other Devices by Milestone Scientific, Inc.

K161883CompuFlo Epidural Computer Controlled Anesthesia System

Related Devices (Code: FMF)

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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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