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FDA 510(k)

UltraFlo-R Push Button Blood Collection Set

K-Number: K220458 · 2023-09-29

ApplicantInnovative Medical Technologies, Inc.
Decision Date2023-09-29
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UltraFlo-R Push Button Blood Collection Set is a medical device manufactured by Innovative Medical Technologies, Inc.. It received FDA 510(k) clearance on 2023-09-29 under approval number K220458. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UltraFlo-R Push Button Blood Collection Set?

UltraFlo-R Push Button Blood Collection Set is a medical device that received FDA 510(k) clearance on 2023-09-29. It is manufactured by Innovative Medical Technologies, Inc.. The 510(k) number is K220458.

When was UltraFlo-R Push Button Blood Collection Set approved by the FDA?

UltraFlo-R Push Button Blood Collection Set received FDA 510(k) clearance on 2023-09-29, under approval number K220458.

What company makes UltraFlo-R Push Button Blood Collection Set?

UltraFlo-R Push Button Blood Collection Set is manufactured by Innovative Medical Technologies, Inc..

What is the FDA product code for UltraFlo-R Push Button Blood Collection Set?

The FDA product code for UltraFlo-R Push Button Blood Collection Set is JKA.

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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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